US20080268204A1 - Multiple layer polymer interlayers having an embossed surface - Google Patents

Multiple layer polymer interlayers having an embossed surface Download PDF

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Publication number
US20080268204A1
US20080268204A1 US11/741,765 US74176507A US2008268204A1 US 20080268204 A1 US20080268204 A1 US 20080268204A1 US 74176507 A US74176507 A US 74176507A US 2008268204 A1 US2008268204 A1 US 2008268204A1
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United States
Prior art keywords
polymer layer
polymer
interlayer
layer
layers
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Abandoned
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US11/741,765
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English (en)
Inventor
David Paul Bourcier
John Joseph D'Errico
Jean-Pierre Etienne
Gary Matis
Vincent James Yacovone
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Solutia Inc
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Solutia Inc
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Priority to US11/741,765 priority Critical patent/US20080268204A1/en
Assigned to SOLUTIA INC. reassignment SOLUTIA INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: D'ERRICO, JOHN JOSEPH, BOURCIER, DAVID PAUL, MATIS, GARY, YACOVONE, VINCENT JAMES, ETIENNE, JEAN-PIERRE
Priority to TW097114518A priority patent/TWI477398B/zh
Priority to KR1020147031190A priority patent/KR101507294B1/ko
Priority to CA2682529A priority patent/CA2682529C/en
Priority to CN200880013717.2A priority patent/CN101668630B/zh
Priority to MX2009011660A priority patent/MX2009011660A/es
Priority to JP2010506547A priority patent/JP5415402B2/ja
Priority to KR20097023279A priority patent/KR20100016325A/ko
Priority to EP08746979A priority patent/EP2150406A1/en
Priority to RU2009136518/05A priority patent/RU2469864C2/ru
Priority to CN201410159331.XA priority patent/CN103921509B/zh
Priority to PCT/US2008/061688 priority patent/WO2008134594A1/en
Priority to BRPI0810998-2A2A priority patent/BRPI0810998A2/pt
Priority to AU2008245544A priority patent/AU2008245544A1/en
Publication of US20080268204A1 publication Critical patent/US20080268204A1/en
Assigned to CITIBANK, N.A. reassignment CITIBANK, N.A. ABL PATENT SECURITY AGREEMENT Assignors: CPFILMS INC., FLEXSYS AMERICA L.P., SOLUTIA INC.
Assigned to CITIBANK, N.A. reassignment CITIBANK, N.A. TERM LOAN PATENT SECURITY AGREEMENT Assignors: CPFILMS INC., FLEXSYS AMERICA L.P., SOLUTIA INC.
Priority to US12/509,107 priority patent/US7883761B2/en
Priority to NO20093092A priority patent/NO20093092L/no
Priority to IL201761A priority patent/IL201761A/en
Assigned to CPFILMS INC., SOLUTIA INC., FLEXSYS AMERICA L.P. reassignment CPFILMS INC. RELEASE OF ABL SECURITY INTEREST IN PATENTS - REEL/FRAME 022610/0495 Assignors: CITIBANK, N.A.
Assigned to FLEXSYS AMERICA L.P., SOLUTIA INC., CPFILMS INC. reassignment FLEXSYS AMERICA L.P. RELEASE OF TERM LOAN SECURITY INTEREST IN PATENTS - REEL/FRAME 022610/0697 Assignors: CITIBANK, N.A.
Assigned to DEUTSCHE BANK TRUST COMPANY AMERICAS, AS COLLATERAL AGENT reassignment DEUTSCHE BANK TRUST COMPANY AMERICAS, AS COLLATERAL AGENT SECURITY AGREEMENT Assignors: CP FILMS INC., FLEXSYS AMERICA L.P., SOLUTIA INC.
Assigned to SOLUTIA INC. reassignment SOLUTIA INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: LU, JUN
Abandoned legal-status Critical Current

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    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
    • B32B17/06—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
    • B32B17/10—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
    • B32B17/10005—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
    • B32B17/1055—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer
    • B32B17/10559—Shape of the cross-section
    • B32B17/10577—Surface roughness
    • B32B17/10587—Surface roughness created by embossing
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
    • B32B17/06—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
    • B32B17/10—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
    • B32B17/10005—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
    • B32B17/1055—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer
    • B32B17/10761—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer containing vinyl acetal
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • 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
    • B32B3/26—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 a particular shape of the outline of the cross-section of a continuous layer; characterised by a layer with cavities or internal voids ; characterised by an apertured layer
    • B32B3/30—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 a particular shape of the outline of the cross-section of a continuous layer; characterised by a layer with cavities or internal voids ; characterised by an apertured layer characterised by a layer formed with recesses or projections, e.g. hollows, grooves, protuberances, ribs
    • 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
    • B32B37/00—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding
    • B32B37/14—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the properties of the layers
    • B32B37/15—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the properties of the layers with at least one layer being manufactured and immediately laminated before reaching its stable state, e.g. in which a layer is extruded and laminated while in semi-molten state
    • B32B37/153—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the properties of the layers with at least one layer being manufactured and immediately laminated before reaching its stable state, e.g. in which a layer is extruded and laminated while in semi-molten state at least one layer is extruded and immediately laminated while in semi-molten state
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B38/00—Ancillary operations in connection with laminating processes
    • B32B38/06—Embossing
    • C—CHEMISTRY; METALLURGY
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C27/00—Joining pieces of glass to pieces of other inorganic material; Joining glass to glass other than by fusing
    • C03C27/06—Joining glass to glass by processes other than fusing
    • C03C27/10—Joining glass to glass by processes other than fusing with the aid of adhesive specially adapted for that purpose
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2250/00—Layers arrangement
    • B32B2250/03—3 layers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2329/00—Polyvinylalcohols, polyvinylethers, polyvinylaldehydes, polyvinylketones or polyvinylketals
    • B32B2329/06—PVB, i.e. polyinylbutyral
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
    • Y10T428/24355—Continuous and nonuniform or irregular surface on layer or component [e.g., roofing, etc.]
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
    • Y10T428/24355—Continuous and nonuniform or irregular surface on layer or component [e.g., roofing, etc.]
    • Y10T428/24372—Particulate matter
    • Y10T428/24405—Polymer or resin [e.g., natural or synthetic rubber, etc.]
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
    • Y10T428/24479—Structurally defined web or sheet [e.g., overall dimension, etc.] including variation in thickness
    • Y10T428/24612—Composite web or sheet
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/25—Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
    • Y10T428/254—Polymeric or resinous material
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
    • Y10T428/31627—Next to aldehyde or ketone condensation product
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
    • Y10T428/31627—Next to aldehyde or ketone condensation product
    • Y10T428/3163—Next to acetal of polymerized unsaturated alcohol [e.g., formal butyral, etc.]
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31942—Of aldehyde or ketone condensation product
    • Y10T428/31946—Next to second aldehyde or ketone condensation product

Definitions

  • the present invention is in the field of polymer interlayers and multiple layer glass panels comprising polymer interlayers, and, more specifically, the present invention is in the field of polymer interlayers comprising multiple thermoplastic polymer layers.
  • Safety glass often refers to a transparent laminate comprising a poly(vinyl butyral) layer disposed between two sheets of glass.
  • Safety glass often is used to provide a transparent barrier in architectural and automotive openings. Its main function is to absorb energy, such as that caused by a blow from an object, without allowing penetration through the opening or the dispersion of shards of glass, thus minimizing damage or injury to the objects or persons within an enclosed area.
  • Safety glass also can be used to provide other beneficial effects, such as to attenuate acoustic noise, reduce UV and/or IR light transmission, and/or enhance the appearance and aesthetic appeal of window openings.
  • thermoplastic polymer found in safety glass can consist of a single layer of a thermoplastic polymer, such as poly(vinyl butyral), or multiple layers. Multiple layers are useful, for example, in acoustic applications. Conventional attempts at such acoustic dampening have included using thermoplastic polymers with low glass transition temperatures. Other attempts have included using two adjacent layers of thermoplastic polymer wherein the layers have dissimilar characteristics (see, for example U.S. Pat. Nos. 5,340,654 and 5,190,826, and U.S. Patent Application 2003/0139520 A1).
  • compositions and methods are needed to enhance the production and optical characteristics of multiple layer glass panels, and specifically multiple layer glass panels comprising multiple layer interlayers.
  • the present invention provides multiple layer interlayers having a relatively soft inner layer and relatively stiff outer layers that can be laminated without unacceptable optical distortion and used in various multiple layer glass panel type applications.
  • Multiple layer interlayers of the present invention have surface topography that is formed by embossing the exposed surface of the interlayer, or individual layers of the multiple layer interlayer, after formation of the interlayer or layers.
  • the embossing process is carried out under temperature conditions that prevent the transfer of the embossing to inner layers of the interlayer.
  • FIG. 1 represents a schematic cross sectional view of a multiple manifold coextrusion device of the present invention.
  • the present invention is directed to multiple layer interlayers that are useful in laminated glass applications in which a softer inner polymer layer is disposed between and in contact with more rigid outer layers, for example in applications in which sound suppression is particularly desirable.
  • acoustic interlayers of the present invention comprise multiple layers, with a preferred embodiment having a relatively soft layer sandwiched between two relatively stiff layers.
  • the resulting three layer interlayer can generally be used in lamination processes directly in place of conventional, single layer interlayers, with little or no modification to the lamination process.
  • the invention includes multiple layer interlayers—for example three layer interlayers—having an inner polymer layer that is softer than the outer layers between which it is disposed, which includes non-acoustic multiple layer interlayers.
  • the present invention it has now been surprisingly discovered that deairing and lamination of multiple layer interlayers can be facilitated by embossing the outer surfaces of a multiple layer interlayer without thereby also creating optical distortion in the glazing panel in which the interlayer is used.
  • This result is accomplished by allowing the multiple layer interlayer to cool after initial extrusion, for example after coextrusion of a three polymer layer interlayer, and prior to embossing.
  • the interlayer in various embodiments, is cooled below 90° C., 80° C., 70° C., or 60° C. In a preferred embodiment, the interlayer is cooled below 60° C.
  • continuously unwound polymer in rolled form, or directly from the die is fed as a single layer to an embossing station having an embossing roll pressing against a rubber-faced backup roll 10 to 60 centimeters (4′′ to 24′′) in diameter at any suitable speed, for example at 305-915 centimeters per minute (10-30 feet per minute).
  • the shaping surface of the embossing roll can be engraved with any desirable surface pattern. In one embodiment, for example, the entire shaping surface of the embossing roll is engraved with a sawtooth configuration.
  • a sawtooth configuration is V-shaped in vertical cross section with the sides of immediately adjacent sawteeth at ninety degrees to each other.
  • the sawteeth form continuous helical ridges on the roll surface, which can be oriented at 45 degrees with respect to the longitudinal roll axis.
  • the frequency of the ridges can be, for example, 127 to 508 per centimeter, or 203 to 508 per centimeter (50 to 200 per inch or 80 to 200 per inch) as measured across the direction of the helix.
  • the face of the cooperating backup roll can be covered with a high extensibility, temperature-resistant rubber capable of stretching without fracturing.
  • the surface of the embossing roll is regulated to the desired temperature, for example, 121° C. to 232° C. (250° F. to 450° F.), 138° C. to 216° C. (280° F. to 420° F.), or 149° C. to 204° C. (300° F. to 400° F.) by the presence of an appropriate heating medium beneath the embossing surface.
  • a vacuum roll downstream of the nip formed by the embossing and backup rolls can be used to pull the embossed layer from the embossing roll surface.
  • the layer after passing through the nip, can be removed by the vacuum roll beyond the nip, and then can be passed with high wrap (>135 degrees) over a chilled cooling roll (below 4.44° C. (40° F.)) and then wound into a roll.
  • embossing two sides of an interlayer can be accomplished by passing the interlayer through the same embossing set up a second time, or through a similar, second set up down line.
  • the interlayer can be embossed by heating the outside surfaces of the interlayer to any suitable temperature and at any suitable speed that does not cause the transfer of the embossing pattern into the soft layer/stiff layer interface.
  • Temperatures can be, for example, 121° C. to 232° C. (250° F. to 450° F.), 138° C. to 216° C. (280° F. to 420° F.), or 149° C. to 204° C. (300° F. to 400° F.), and those temperatures can be attained, for example, by processing the interlayer through embossed rollers heated to the desired temperature and having the desired embossing pattern.
  • the embossed pattern is effectively kept from pushing through the outer stiffer layers and into the interface between the outer layer and the inner layer at the time of embossing and then later, at the time of lamination. It is the distortion of that interface through embossing and/or laminating that is believed to cause optical distortion in laminates, as has been reported in some prior art (see, for example, EP 0 710 545 A1). Indeed, where that prior art warns against embossing too deeply, multiple layer interlayers of the present invention are not so restricted and, as will be described in detail below, can be embossed well beyond the limits proposed in the prior art.
  • Embossing is a method of providing a roughened deairing surface to a polymer interlayer or layer (see, for example, U.S. Pat. Nos. 5,425,977 and 6,077,374).
  • Conventional techniques for embossing a polymer layer include passing the layer through a nip between two rotating rolls, one or both of which are embossing rolls having indentations formed in its surface which are complementarily-shaped negatives of the desired embossment pattern (see, for example, U.S. Pat. Nos. 4,671,913; 2,904,844; 2,909,810; 3,994,654; 4,575,540; 5,151,234 and European Application No. 0185,863).
  • Embossing patterns can be regular or random, depending on the application.
  • One or both surfaces of the outer polymer layers of the interlayer are produced using embossing to produce a layer having the desired “roughness”, or “R Z ”, “pitch”, or R SM , and permanence.
  • R Z is a measure of the surface topography of a polymer layer and is an indication of divergence of the surface from a plane.
  • R SM is a measure of the distance between peaks in the topography of the surface of a polymer layer.
  • Perfect is a measure of the tendency of the surface of the embossed interlayer to resist the memory inherent in the layer, which results in a tendency of the surface to return to the surface topography that existed prior to embossing. The three measurements will be described in detail, below.
  • a multiple layer interlayer having a softer inner polymer layer is produced using the embossing techniques taught herein in which one or both of the outer surfaces of the interlayer have an R Z value of 50 to 90, 60 to 90, or 60 to 80.
  • the two outer surfaces can have the same R Z value or a different value.
  • only one of the two outer surfaces has the designated R Z value.
  • either one or both of the outer layers of an interlayer have the designated R Z value on the inner surface, which is disposed in contact with an inner, relatively soft layer, which is found, for example, in non-coextrusion embodiments in which multiple individual layers are laminated together to form a multiple layer interlayer.
  • the outer surfaces of an interlayer of the present invention have an R SM value of less than 700, 650, or 600. In further embodiments, only one outer surface has the designated R SM value. In yet other embodiments, one or both of the inner surfaces of the outer layers of an interlayer have the designated R SM value.
  • the R SM values given can be combined with the R Z values given in any suitable combination to produce the desired surface characteristics.
  • Multiple layer interlayers of the present invention in various embodiments, have a “permanence value”, which will be described in detail below, of less than 95%, less than 90%, less than 80%, less than 70%, or less than 60%, and these permanence values, again, can be combined with any of the given R SM values and R Z values in any suitable combination to produce the desired surface characteristics.
  • permanence values of one or both outer surfaces are 40% to 95% or 50% to 90%.
  • Examples of preferred combinations of the three surface characteristics for one or both surfaces of the multiple layer interlayers of the present invention include, without limitation, the following combinations, which are arranged in the order R Z ///R SM ///permanence and are separated by semicolons, and where R Z and R SM are given in microns and permanence is given as a percentage: 50 to 90////any////less than 95; 50 to 90////any////less than 90; 50 to 90////40 to 95; 50 to 90////less than 700////less than 95; 50 to 90///less than 700///less than 90; 50 to 90///less than 700///40 to 95; 60 to 80///any////less than 95; 60 to 80////any////less than 90; 60 to 80////any///40 to 95; 60 to 80////less than 700///less than 95; 60 to 80///less than 700///less than
  • the resulting interlayer, with the specified R Z and/or R SM and/or permanence value can be readily laminated between two glazing layers such as glass.
  • superior sound suppression characteristics can be imparted to multiple layer glass panels by incorporating a multiple layer interlayer into the panels, where the interlayer comprises two polymer layers having different plasticizer concentrations.
  • interlayers of the present invention will be usable in many applications without requiring any modification to the manufacturing method used in the applications.
  • automotive windshield applications can involve the use of a conventional polymeric interlayer that can be replaced with an interlayer of the present invention without altering the lamination process used to form the finished windshield.
  • an “interlayer” is any thermoplastic construct that can be used in multiple layer glass applications, such as safety glass in windshields and architectural windows
  • a “multiple layer” interlayer is any interlayer that is formed by combining, usually through laminating processes or coextrusion, two or more individual layers into a single interlayer.
  • a multiple layer interlayer comprises two polymer layers disposed in contact with each other, wherein each polymer layer comprises a thermoplastic polymer, as detailed elsewhere herein.
  • the thermoplastic polymer can be the same or different in each layer.
  • a high plasticizer content polymer layer is sandwiched between two low plasticizer content layers to form a three layer interlayer.
  • the composition of the polymer layers is such that net migration of plasticizer from one polymer layer to another is negligible or zero, thereby maintaining the plasticizer differential.
  • plasticizer content can be measured as parts per hundred resin (phr) parts, on a weight per weight basis. For example, if 30 grams of plasticizer is added to 100 grams of polymer resin, then the plasticizer content of the resulting plasticized polymer would be 30 phr. As used herein throughout, when the plasticizer content of a polymer layer is given, the plasticizer content of that particular layer is determined with reference to the phr of the plasticizer in the melt that was used to produce that particular layer.
  • the plasticizer content can be determined via a wet chemical method in which an appropriate solvent, or a mixture of solvents, is used to extract the plasticizer out of the layer.
  • an appropriate solvent or a mixture of solvents
  • the plasticizer content in phr can be calculated.
  • one polymer layer can be physically separated from the other before the plasticizer content in each of the polymer layers is measured.
  • the plasticizer content of the two polymer layers differ by at least 8 phr, 10 phr, 12 phr, 15 phr, 18 phr, 20 phr, or 25 phr.
  • Each layer can have, for example 30 to 100 phr, 40 to 90 phr, or 50 to 80 phr.
  • residual hydroxyl contents of the thermoplastic polymer components of the polymer layers are different, which allows for the fabrication of layers with stable plasticizer differences.
  • residual hydroxyl content refers to the amount of hydroxyl groups remaining as side groups on the polymer chains after processing is complete.
  • poly(vinyl butyral) can be manufactured by hydrolyzing poly(vinyl acetate) to poly(vinyl alcohol), and then reacting the poly(vinyl alcohol) with butyraldehyde to form poly(vinyl butyral).
  • the residual hydroxyl content of the two adjacent polymer layers can differ by at least 1.8%, 2.0%, 2.2%, 2.5%, 3.0%, 4.0%, 5.0%, 7.5%, or by at least 10%. This difference is calculated by subtracting the residual hydroxyl content of the layer with the lower residual hydroxyl content from the residual hydroxyl content of the layer with the greater residual hydroxyl content. For example, if a first polymer layer has a residual hydroxyl content of 20 weight percent, and a second polymer layer has a residual hydroxyl content of 17 weight percent, then the residual hydroxyl content of the two layers differs by 3 weight percent.
  • the compatibility of that plasticizer in a poly(vinyl butyral) is largely determined by the hydroxyl content.
  • poly(vinyl butyral) with a greater residual hydroxyl content will result in a reduced plasticizer compatibility or capacity.
  • poly(vinyl butyral) with a lower residual hydroxyl content will result in an increased plasticizer compatibility or capacity.
  • residual hydroxyl content can be controlled by controlling reaction times, reactant concentrations, and other variables in the manufacturing process.
  • the residual hydroxyl content of the two layers is as follows: first layer less than 25% and second layer less than 23%; first layer less than 23% and second layer less than 21%; first layer less than 21% and second layer less than 19%; first layer less than 20% and second layer less than 17%; first layer less than 18% and second layer less than 15%; first layer less than 15% and second layer less than 12%.
  • any of the values given in a previous paragraph for the difference in hydroxyl content between the two layers can be used.
  • the relative terms “soft/softer” and “stiff/stiffer” refer to the tensile break stress of the polymer layer.
  • tensile break stress, or tensile strength, of a polymer layer is defined and measured according to the method described in JIS K6771, with a relatively “soft” polymer layer having a lower tensile break stress value than a relatively “stiff” polymer layer.
  • two polymer layers have a tensile break stress according to the following, wherein the first polymer layer in the following list is the polymer layer with the lower plasticizer content: first polymer layer greater than 135 kilograms per square centimeter and second polymer layer less than 120 kilograms per square centimeter; first polymer layer greater than 150 kilograms per square centimeter and second polymer layer less than 135 kilograms per square centimeter; first polymer layer greater than 165 kilograms per square centimeter and second polymer layer less than 150 kilograms per square centimeter; or first polymer layer greater than 180 kilograms per square centimeter and second polymer layer less than 165 kilograms per square centimeter.
  • a third polymer layer disposed in contact with the second polymer layer opposite the first polymer layer so as to sandwich the second polymer layer between the first and third polymer layers, can be added to any of the above embodiments, with the third layer having the same or different composition as the first polymer layer, and preferably having the same composition as the first polymer layer.
  • tensile break stress values provided in the preceding paragraph represent values that could be used for acoustic type multiple layer interlayers
  • those of skill in the art will recognize that the methods and interlayers of the present invention are useful for any multiple layer interlayer having a relatively soft inner layer and one or more relatively stiff outer layers.
  • one or both outer layers have a tensile break stress that is an least 15 kilograms per square centimeter, 20 kilograms per square centimeter, or 25 kilograms per square centimeter greater than the tensile break stress of a softer inner layer.
  • a conventional laminated glass is formed through laminating a conventional interlayer, which is typically used today for commercial laminated glass, wherein the conventional interlayer has a tensile break stress of 200 kilograms per square centimeter or higher.
  • conventional laminated glass is referred to as a “reference laminate panel” or “reference panel.”
  • the “combined glass thickness” is the sum of the thickness of the two layers of glass; in more complex laminates with three or more layers of glass, the combined glass thickness would be the sum of the three or more layers of glass.
  • a “coincident frequency” means the frequency at which a panel exhibit a dip in sound transmission loss due to “coincident effect”.
  • the coincident frequency of the reference panel is typically in the range of 2,000 to 6,000 Hertz, and can be empirically determined from a monolithic sheet of glass having a thickness equal to the combined glass thickness of glass in the reference panel from the algorithm
  • improvement in acoustic performance can be measured by an increase in sound transmission loss at the coincident frequency (reference frequency) of the reference panel.
  • Solid transmission loss is determined for a laminate of the present invention or conventional reference panel of fixed dimensions with ASTM E90 (95) at a fixed temperature of 20° C.
  • multiple layer interlayers of the present invention when laminated between two panes of glass sheet, reduce the transmission of sound through the laminated glass panel by at least 2 decibels (dB) relative to a comparable reference panel having a single conventional interlayer with a thickness comparable to that of the multiple layer interlayer of the present invention.
  • interlayers of the present invention when laminated between two sheets of glass, improve the sound transmission loss by at least 2 dB, more preferably 4 dB, more preferably 6 dB or higher, and even more preferably 8 dB or higher at the reference frequency relative to a comparable reference panel.
  • two adjacent polymer layers of the present invention have the differing plasticizer content as described above, and each further can have a residual acetate content of less than 5 mole %, less than 4 mole %, less than 3 mole %, less than 2 mole %, or less than 1 mole %.
  • These residual acetate concentrations can be combined with the residual hydroxyl contents given above, in any combination, to form two polymer layers of the present invention having the described differences in plasticizer content and residual hydroxyl content while having little to no residual acetate content.
  • multiple layer interlayers of the present invention include interlayers having more than two polymer layers, wherein one or more of the additional polymer layers has a residual acetate content of less than 5 mole %, less than 4 mole %, less than 3 mole %, less than 2 mole %, or less than 1 mole %.
  • FIG. 1 Foregoing embodiments, include any of the foregoing embodiments further comprising a third polymer layer that is disposed in contact with the softer polymer layer, for example, the one having the higher plasticizer content. Addition of this third polymer layer results in a three layer construct that has the following structure: First polymer layer that is relatively stiff//Second polymer layer that is relatively soft//Third polymer layer.
  • This third polymer layer can have the same composition as the first polymer layer, as it does in preferred embodiments, or it can be different.
  • the preferred embodiments of the present invention have a soft inner layer disposed between an in contact with two stiffer outer layers, it will be understood by those of skill in the art that the methods of the present invention can also be applied to two layer interlayers and interlayers having more than three layers. For example, a variation within the scope of the present invention would be a five layer interlayer having two stiffer outer layers and three inner softer layers.
  • the third polymer layer has the same composition as the first polymer layer, which provides a three layer interlayer that has a relatively difficult to handle polymer layer disposed between two relatively easy to handle layers, resulting in a multiple layer interlayer that is relatively easy to handle and which can be incorporated directly into existing processes that previously used a single polymer layer having the composition of the outer two polymer layers of the interlayer of the present invention, or a composition that results in similar processing characteristics (for example, blocking tendency).
  • the third polymer layer has a different composition than the first polymer layer, and the differences in composition between the third polymer layer and the second polymer layer can be any of the differences given above for the differences between the first polymer layer and the second polymer layer.
  • the third polymer layer differs from the second polymer layer at least in that it has a residual hydroxyl content that is 2% greater than the hydroxyl content of the second polymer layer.
  • any of the other differences noted herein throughout can singly or in combination distinguish the third polymer layer from the second polymer layer.
  • interlayers of the present invention can be incorporated into the interlayers of the present invention.
  • polymer films such as polyesters like poly(ethylene terephthalate) having a metallized layer, an infrared reflecting stack, or other performance layer deposited thereon, can be included between any two polymer layers of the present invention, where appropriate.
  • an interlayer can be fabricated with the following layout: polymer layer with relatively high plasticizer content//polyester film having a performance layer//polymer layer with relatively low plasticizer content.
  • additional layers of thermoplastics, such as poly(vinyl butyral), polyester films, primer layers, and hardcoat layers can be added to the multiple layer interlayers of the present invention according to the desired result and the particular application.
  • the preferred method of producing interlayers of the present invention is through the simultaneous coextrusion of multiple, for example three, polymer layers.
  • coextrusion of multiple melts results in multiple polymer layers being formed together as one interlayer.
  • Multiple layer interlayers of the present invention are preferably coextruded using a multiple manifold coextrusion device such as the one shown in FIG. 1 .
  • an extrusion device has a first die manifold 12 a second die manifold 14 , and a third die manifold 16 .
  • the device shown in FIG. 1 operates by simultaneously extruding polymer melts from each manifold ( 12 , 14 , 16 ) toward the extrusion opening 20 , where the multiple layer interlayer is extruded as a composite of three individual polymer layers. Layer thickness can be varied by adjusting the distance between the die lips at the extrusion opening 20 .
  • a “polymer layer” includes layers that are produced individually and layers that are coextruded.
  • an interlayer that is produced by coextruding three melts will have three individual “polymer layers” just as will an interlayer that is produced by laminating three individually produced polymer layers into a single interlayer.
  • the present invention also provides methods of reducing the level of sound through an opening, comprising the step of disposing in the opening a multiple layer glass panel comprising any of the interlayers of the present invention.
  • the present invention also includes methods of manufacturing a multiple layer glazing, comprising laminating any of the interlayers of the present invention between two rigid, transparent panels, as are known in the art, such as glass or acrylic layers.
  • the present invention also includes multiple layer glass panels, such as windshields and architectural windows, comprising a multiple layer interlayer of the present invention.
  • multiple layer glazing panels having plastics, such as acrylics, or other suitable materials in place of the glass panels.
  • the present invention also includes a method of making a polymer interlayer having an internal layer with a relatively low tensile break stress compared to the outside layers by forming a first polymer melt, a second polymer melt, and a third polymer melt, and optionally a fourth or more polymer melts; and, coextruding said first polymer melt, said second polymer melt, and said third polymer to form an interlayer, and, optionally, said fourth or more polymer melts, cooling the interlayer to a suitable temperature, as described elsewhere herein, heating a surface of the interlayer to a suitable temperature, as described elsewhere herein, and, embossing said surface of said interlayer to an R Z of 20 to 90, or 20-70.
  • R SM and the permanence value can be any as given elsewhere herein.
  • preferred combinations of the three surface characteristics for one or both surfaces of the multiple layer interlayers of the present invention include, without limitation, the following combinations, which are arranged in the order R Z ///R SM ///permanence and are separated by semicolons, and where R Z and R SM are given in microns and permanence is given as a percentage: 20 to 90////any////less than 95; 20 to 90////any////less than 90; 20 to 90////any////40 to 95; 20 to 90////less than 700////less than 95; 20 to 90///less than 700////less than 90; 20 to 90///less than 700///40 to 95; 20-70////any////less than 95; 20-70////any////less than 90; 20-70////any////40 to 95; 20-70////
  • a “polymer film” means a relatively thin and rigid polymer layer that functions as a performance enhancing layer.
  • Polymer films differ from polymer layers, as used herein, in that polymer films do not themselves provide the necessary penetration resistance and glass retention properties to a multiple layer glazing structure, but rather provide performance improvements, such as infrared absorption character.
  • Poly(ethylene terephthalate) is most commonly used as a polymer film.
  • the polymer film layer has a thickness of 0.013 mm to 0.20 mm, preferably 0.025 mm to 0.1 mm, or 0.04 to 0.06 mm.
  • the polymer film layer can optionally be surface treated or coated to improve one or more properties, such as adhesion or infrared radiation reflection.
  • These functional performance layers include, for example, a multi-layer stack for reflecting infra-red solar radiation and transmitting visible light when exposed to sunlight. This multi-layer stack is known in the art (see, for example, WO 88/01230 and U.S. Pat. No.
  • 4,799,745) and can comprise, for example, one or more Angstroms-thick metal layers and one or more (for example two) sequentially deposited, optically cooperating dielectric layers.
  • the metal layer(s) may optionally be electrically resistance heated for defrosting or defogging of any associated glass layers.
  • An additional type of polymer film that can be used with the present invention which is described in U.S. Pat. No. 6,797,396, comprises a multitude of nonmetallic layers that function to reflect infrared radiation without creating interference that can be caused by metallic layers.
  • the polymer film layer in some embodiments, is optically transparent (i.e. objects adjacent one side of the layer can be comfortably seen by the eye of a particular observer looking through the layer from the other side), and usually has a greater, in some embodiments significantly greater, tensile modulus regardless of composition than that of any adjacent polymer layer.
  • the polymer film layer comprises a thermoplastic material.
  • thermoplastic materials having suitable properties are nylons, polyurethanes, acrylics, polycarbonates, polyolefins such as polypropylene, cellulose acetates and triacetates, vinyl chloride polymers and copolymers and the like.
  • the polymer film layer comprises materials such as re-stretched thermoplastic films having the noted properties, which include polyesters, for example poly(ethylene terephthalate) and poly(ethylene terephthalate) glycol (PETG).
  • polyesters for example poly(ethylene terephthalate) and poly(ethylene terephthalate) glycol (PETG).
  • poly(ethylene terephthalate) is used, and, in various embodiments, the poly(ethylene terephthalate) has been biaxially stretched to improve strength, and has been heat stabilized to provide low shrinkage characteristics when subjected to elevated temperatures (e.g. less than 2% shrinkage in both directions after 30 minutes at 150° C.).
  • Poly(ethylene terephthalate) film that can be used with the present invention are disclosed in published European Application No. 0157030.
  • Polymer films of the present invention can also include a hardcoat and/or and antifog layer, as are known in the art.
  • a “polymer layer” means any thermoplastic polymer composition formed by any suitable method into a thin layer that is suitable alone, or in stacks of more than one layer, for use as an interlayer that provides adequate penetration resistance and glass retention properties to laminated glazing panels. Plasticized poly(vinyl butyral) is most commonly used to form polymer layers.
  • the polymer layer can comprise any suitable polymer, and, in a preferred embodiment, the polymer layer comprises poly(vinyl butyral).
  • the polymer layer comprises poly(vinyl butyral).
  • the polymer component consists of or consists essentially of poly(vinyl butyral).
  • any of the variations in additives disclosed herein can be used with the polymer layer having a polymer consisting of or consisting essentially of poly(vinyl butyral).
  • the polymer layer comprises a polymer based on partially acetalized poly(vinyl alcohol)s.
  • the polymer layer comprises a polymer selected from the group consisting of poly(vinyl butyral), polyurethane, polyvinyl chloride, poly(ethylene vinyl acetate), combinations thereof, and the like.
  • the polymer layer comprises plasticized poly(vinyl butyral).
  • the polymer layer comprises poly(vinyl butyral) and one or more other polymers. Other polymers having a proper plasticizing capacity can also be used.
  • the poly(vinyl butyral) can be produced by known acetalization processes that involve reacting poly(vinyl alcohol) with butyraldehyde in the presence of an acid catalyst, followed by neutralization of the catalyst, separation, stabilization, and drying of the resin, with the understanding that in various embodiments, residual hydroxyl content will be controlled, as described elsewhere herein.
  • the polymer layer comprises poly(vinyl butyral) having a molecular weight greater than 30,000, 40,000, 50,000, 55,000, 60,000, 65,000, 70,000, 120,000, 250,000, or 350,000 grams per mole (g/mole or Daltons). Small quantities of a dialdehyde or trialdehyde can also be added during the acetalization step to increase molecular weight to greater than 350,000 Daltons (see, for example, U.S. Pat. Nos. 4,874,814; 4,814,529; and 4,654,179). As used herein, the term “molecular weight” means the weight average molecular weight.
  • plasticizer has a hydrocarbon segment of fewer than 20, fewer than 15, fewer than 12, or fewer than 10 carbon atoms.
  • Plasticizers used in the polymer layers of the present invention can include esters of a polybasic acid or a polyhydric alcohol, among others.
  • Suitable plasticizers include, for example, triethylene glycol di-(2-ethylbutyrate), triethylene glycol di-(2-ethylhexanoate), triethylene glycol diheptanoate, tetraethylene glycol diheptanoate, dihexyl adipate, dioctyl adipate, hexyl cyclohexyladipate, mixtures of heptyl and nonyl adipates, diisononyl adipate, heptylnonyl adipate, dibutyl sebacate, polymeric plasticizers such as the oil-modified sebacic alkyds, and mixtures of phosphates and adipates such as disclosed in U
  • plasticizers that can be used are mixed adipates made from C 4 to C 9 alkyl alcohols and cyclo C 4 to C 10 alcohols, as disclosed in U.S. Pat. No. 5,013,779, and C 6 to C 8 adipate esters, such as hexyl adipate.
  • the plasticizer is triethylene glycol di-(2-ethylhexanoate).
  • Adhesion control agents can also be included in the polymer layers of the present invention to impart the desired adhesiveness. These agents can be incorporated into the outer layers in a three polymer layer embodiment, for example. Any of the ACAs disclosed in U.S. Pat. No. 5,728,472 can be used. Additionally, residual sodium acetate and/or potassium acetate can be adjusted by varying the amount of the associated hydroxide used in acid neutralization.
  • polymer layers of the present invention comprise, in addition to sodium acetate, magnesium bis(2-ethyl butyrate)(chemical abstracts number 79992-76-0). The magnesium salt can be included in an amount effective to control adhesion of the polymer layer to glass.
  • Additives may be incorporated into the polymer layer to enhance its performance in a final product.
  • additives include, but are not limited to, plasticizers, dyes, pigments, stabilizers (e.g., ultraviolet stabilizers), antioxidants, flame retardants, other IR absorbers, anti-block agents, combinations of the foregoing additives, and the like, as are known in the art.
  • Agents that selectively absorb light in the visible or near infrared spectrum can be added to any of the appropriate polymer layers.
  • Agents that can be used include dyes and pigments such as indium tin oxide, antimony tin oxide, or lanthanum hexaboride (LaB 6 ).
  • any suitable method can be used to produce poly(vinyl butyral). Details of suitable processes for making poly(vinyl butyral) are known to those skilled in the art (see, for example, U.S. Pat. Nos. 2,282,057 and 2,282,026). In one embodiment, the solvent method described in Vinyl Acetal Polymers, in Encyclopedia of Polymer Science & Technology, 3 rd edition, Volume 8, pages 381-399, by B. E. Wade (2003) can be used. In another embodiment, the aqueous method described therein can be used. Poly(vinyl butyral) is commercially available in various forms from, for example, Solutia Inc., St. Louis, Mo. as ButvarTM resin.
  • resin refers to the polymeric (for example poly(vinyl butyral)) component that is removed from the mixture that results from the acid catalysis and subsequent neutralization of the polymeric precursors. Resin will generally have other components in addition to the polymer, for example poly(vinyl butyral), such as acetates, salts, and alcohols.
  • melt refers to a mixture of resin with a plasticizer and, optionally, other additives.
  • One exemplary method of forming a poly(vinyl butyral) layer comprises extruding molten poly(vinyl butyral) comprising resin, plasticizer, and additives and then forcing the melt through a sheet die (for example, a die having an opening that is substantially greater in one dimension than in a perpendicular dimension).
  • Another exemplary method of forming a poly(vinyl butyral) layer comprises casting a melt from a die onto a roller, solidifying the resin, and subsequently removing the solidified resin as a sheet.
  • a “prelaminate” interlayer is formed by assembling the individual layers into a stack of layers, and then subjecting the layers to sufficient heat and pressure to tack the layers together, thereby forming the prelaminate.
  • the prelaminate can then be rolled or otherwise stored as desired until it is used in a laminated glazing, at which point the prelaminate is placed between two layers of glass and laminated to form the final multiple layer glazing.
  • the interlayers of the present invention can have total thicknesses of 0.1 to 2.5 millimeters, 0.2 to 2.0 millimeters, 0.25 to 1.75 millimeters, and 0.3 to 1.5 millimeters (mm).
  • the individual polymer layers of a multiple layer interlayer can have, for example, approximately equal thicknesses that, when added together, result in the total thickness ranges given above.
  • the thicknesses of the layers can be different, and can still add to the total thicknesses given above.
  • the outer layers can be 0.18 to 0.36 millimeters
  • the inner layer can be 0.12 to 0.16 millimeters, with a total thickness of 0.51 to 0.89 millimeters.
  • any of the layers, and particularly the outer layers can have a thickness of 0.05 to 0.71 millimeters (2 to 28 mils), 0.05 to 0.64 millimeters (2 to 25 mils), or 0.05 to 0.51 millimeters (2 to 20 mils). These thickness ranges can be combined with any of the values given elsewhere herein for R Z , R SM , and permanence.
  • one or both of the outer layers of a multiple layer interlayer has a thickness of 0.05 to 0.71 millimeters, 0.05 to 0.64 millimeters, or 0.05 to 0.51 millimeters and an R Z of 50 to 90, 60 to 90, or 60 to 80.
  • the parameters for the polymer layer described above apply as well to any layer in a multiple layer construct of the present invention that is a poly(vinyl butyral) type layer.
  • a 15 centimeter by 15 centimeter test sample of plasticized polymer layer is placed on a vacuum plate regulated by fluid at room temperature circulating through it.
  • a vacuum of 3.44 kPa (5 psi) is imposed to draw the sample against the plate surface.
  • a model S8P Perthometer with a PRK drive unit and an RFHTB-250 tracing stylus (available from Mahr Gage Co., New York) is used to directly measure layer surface roughness of each side of the test sample. Profile selection is set to “R” on the instrument.
  • the tracing stylus moves automatically across the sample surface.
  • the length of each trace (L T ) is 17.5 millimeter composed of 7 sequential sample lengths L C of 2.5 mm.
  • the measuring length (L m ) is 12.5 millimeter and is composed of the 5 sequential sample lengths (L C ) obtained by eliminating the first and the last sections of each trace.
  • the average value of individual roughness depths in these five sequential sample lengths L C is determined and R Z is the average of ten such determinations, five taken in the machine direction of extrusion (MD) and five in the cross machine direction (CMD).
  • the distance between two consecutive traces in each direction is 3 mm.
  • R SM the average peak distance, is determined from the same measurement as for R Z .
  • Mean distance of all profile peaks within the each measuring length (L m ) is determined and the reported R SM for each machine direction is the average of five such determinations on that direction.
  • Polymer layers of the present invention are also characterized by their “permanence,” which is determined according to the following technique: For polymer layers that are embossed, a polymer layer is measured for R Z (R Z Base) prior to embossing. After embossing, a second R Z measurement is taken (R Z Final). For polymer layers that are not embossed a roughness measurement, R Z , is taken and designated R Z Final, and R Z Base is given the value zero. For both embossed and non-embossed layers, a 12.7 centimeter square sample is then cut from the polymer layer.
  • Poly(ethylene terephthalate) film is placed on the edges of one half of a wood frame resting on a horizontal surface, wherein the frame periphery is slightly smaller than the polymer layer sample.
  • the polymer layer sample is then placed on the wood frame so that the poly(ethylene terephthalate) film is between the wood frame and the edges of the polymer layer, in which position it prevents the polymer film from adhering to the wood frame, which would make disassembly difficult.
  • a second poly(ethylene terephthalate) film is then place over the polymer layer, and the second half of the wooden frame is then placed on top of the poly(ethylene terephthalate) film.
  • the two frame halves are then clamped together with binder clips, thereby sandwiching the polymer layer between the two poly(ethylene terephthalate) films and the two frame halves.
  • the frame and polymer assembly is then placed in a preheated oven for 5 minutes at 100° C. The assembly is then removed and allowed to cool. Another R Z value is then determined for the polymer layer sample (R Z 100° C.).
  • a permanence value can then be determined according to the following formula:
  • a shadow graph light (a xenon light powered by a kni-tron rectifier (model number R-2120-2) from Kneisley Electric company, Toledo, Ohio) is positioned in a dark room at 1 meter from a white surface.
  • a sample is held between the white surface and the light source next to a “maximum standard level” standard laminate that represents the lowest acceptable optical quality.
  • the image projected on the white surface is visually examined. If the sample image is worse than the maximum standard level standard, then the sample is rejected as having too much distortion. If the sample is at least as good as the maximum standard level standard, then the sample is compared to progressively optically superior standards until a grade is determined for the sample.
  • the sample is evaluated in the cross machine direction and the machine direction, and the worst grade of the two is designated the grade for the sample.
  • a grade of 0 indicates that no optical distortion is visible.
  • a grade of 1 or 2 indicates some minor distortion is observable.
  • a grade of 3 to 4 indicates that more than minor distortion is apparent.
  • a grade of 5 or higher indicates that significant distortion is observable and the laminate would likely be unusable in applications that require visual clarity, such as in automobile windshields.
  • the clarity of a polymer layer, and particularly a poly(vinyl butyral) layer can be determined by measuring the haze value, which is a quantification of the amount of light scattered away from the direction of the incident beam in passing through the layer.
  • the percent haze can be measured according to the following technique.
  • An apparatus for measuring the amount of haze a Hazemeter, Model D25, which is available from Hunter Associates (Reston, Va.), can be used in accordance with ASTM D1003-61 (Re-approved 1977)-Procedure A, using Illuminant C, at an observer angle of 2 degrees.
  • percent haze is less than 5%, less than 3%, and less than 1%.
  • the visible transmittance can be quantified using a UV-Vis-NIR spectrophotometer such as the Lambda 900 made by Perkin Elmer Corp. by methods described in international standard ISO 9050:1990.
  • the transmittance through a polymer layer of the present invention is at least 60%, at least 70%, or at least 80%.
  • Pummel adhesion can be measured according to the following technique, and where “pummel” is referred to herein to quantify adhesion of a polymer layer to glass, the following technique is used to determine pummel.
  • Two-ply glass laminate samples are prepared with standard autoclave lamination conditions. The laminates are cooled to about ⁇ 18° C. (0° F.) and manually pummeled with a hammer to break the glass. All broken glass that is not adhered to the poly(vinyl butyral) layer is then removed, and the amount of glass left adhered to the poly(vinyl butyral) layer is visually compared with a set of standards.
  • the standards correspond to a scale in which varying degrees of glass remain adhered to the poly(vinyl butyral) layer.
  • Poly(vinyl butyral) layers of the present invention can have, for example, a pummel value of between 3 and 10.
  • Tensile break stress can be determined for a polymer layer according to the procedure described in JIS K6771.
  • Each interlayer comprises a 0.1524 millimeter (6 mil) layer sandwiched between two 0.3302 millimeters (13 mil) layers for a total thickness of 0.8128 millimeters (32 mils).
  • the inner layer comprises 75 phr plasticizer (triethylene glycol di-(2-ethylhexanoate)) and 11.0% residual polyvinyl alcohol, while the outside layers comprise 38 phr plasticizer (triethylene glycol di-(2-ethylhexanoate)) and 18.5% residual polyvinyl alcohol.
  • the first interlayer has an R Z of about 20.
  • the second interlayer has an R Z of about 40.
  • the exact R Z values are given in Table 1, where “CMD” is cross machine direction and “MD” is machine direction and where measurements from both sides of each interlayer are shown:
  • Sample A is then cut into four separate interlayers and sample B is also divided into four separate interlayers.
  • Table 2 shows the results for interlayers formed from sample A and from sample B that are embossed at 174° C. (345° F.) at a rate of 7.6 meters (25 feet) per minute.
  • Table 3 shows the results for interlayers formed from sample A and from sample B that are embossed at 193° C. (380° F.) at a rate of 7.6 meters (25 feet) per minute.
  • Table 4 shows the results for interlayers formed from sample A and from sample B that are embossed at 204° C. (400° F.) at a rate of 4.6 meters (15 feet) per minute.
  • Table 5 shows the results for interlayers formed from sample A and from sample B that are embossed at 174° C. (345° F.) at a rate of 7.6 meters (25 feet) per minute.
  • Table 6 shows the results for interlayers formed from sample A and from sample B that are embossed at 193° C. (380° F.) at a rate of 7.6 meters (25 feet) per minute.
  • Table 7 shows the results for interlayers formed from sample A and from sample B that are embossed at 204° C. (400° F.) at a rate of 4.6 meters (15 feet) per minute.
  • the six embossed samples, as well as the two samples that are unembossed, are placed between two panes of glass and laminated.
  • Lamination is a multistep process in which the poly(vinyl butyral) sheets and glass are converted to a combined final form of safety glass having desirable performance and optical clarity characteristics.
  • Vacuum bag deairing is a technique that is used to evacuate air from a rigid substrate/interlayer/rigid substrate construction prior to the final step of autoclaving. It frequently can be employed to improve autoclave yields in commercial operations. Samples are placed in a resilient rubber bag, which is then evacuated by a vacuum hose mated to the bag. In one embodiment, the bag is brought up to and held at a temperature of about 50° C. for 60 minutes and then to 120° C. for 20 minutes while under vacuum. The bag is then cooled and the resulting panel is removed and placed in an autoclave for final finishing.
  • Light transmission measurements are taken after vacuum bag deairing and before autoclaving. A higher number indicates low cloudiness, which means that little or no air remains in the rigid substrate/interlayer/rigid substrate construct.
  • Light transmission is tested with an adhesion photometer (Tokyo Denshoku #S-904356. Each laminate is tested eight times at dispersed locations throughout the laminate, and the eight results are averaged to give light transmission, as shown in Table 9, where LT is light transmission.
  • Mottle is determined as described elsewhere herein, with results from 5 observers averaged to provide a final mottle grade. Results are shown in Table 10, where “Smp” is sample, “MD” is machine direction, “CMD” is cross machine direction, and “Final” is the mottle grade, which is the greater of the machine direction and cross machine direction results.
  • any of the ranges, values, or characteristics given for any single component of the present invention can be used interchangeably with any ranges, values, or characteristics given for any of the other components of the invention, where compatible, to form an embodiment having defined values for each of the components, as given herein throughout.
  • a polymer layer can be formed comprising residual acetate content in any of the ranges given in addition to any of the ranges given for plasticizer, as well as having any of the R Z , R SM , and permanence values given, where appropriate, to form many permutations that are within the scope of the present invention but that would be cumbersome to list.

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US11/741,765 US20080268204A1 (en) 2007-04-29 2007-04-29 Multiple layer polymer interlayers having an embossed surface
TW097114518A TWI477398B (zh) 2007-04-29 2008-04-21 具有浮凸表面之多層聚合物內層
RU2009136518/05A RU2469864C2 (ru) 2007-04-29 2008-04-25 Многослойные полимерные промежуточные слои с тисненой поверхностью
CN201410159331.XA CN103921509B (zh) 2007-04-29 2008-04-25 具有压花表面的多层聚合物中间层
AU2008245544A AU2008245544A1 (en) 2007-04-29 2008-04-25 Multiple layer polymer interlayers having an embossed surface
CN200880013717.2A CN101668630B (zh) 2007-04-29 2008-04-25 具有压花表面的多层聚合物中间层
MX2009011660A MX2009011660A (es) 2007-04-29 2008-04-25 Capas intermedias de polimero de capas multiples que tienen una superficie estampada.
JP2010506547A JP5415402B2 (ja) 2007-04-29 2008-04-25 エンボス表面を有する複数層ポリマー中間層
KR20097023279A KR20100016325A (ko) 2007-04-29 2008-04-25 엠보싱 표면을 갖는 다층 폴리머 중간층들
EP08746979A EP2150406A1 (en) 2007-04-29 2008-04-25 Multiple layer polymer interlayers having an embossed surface
CA2682529A CA2682529C (en) 2007-04-29 2008-04-25 Multiple layer polymer interlayers having an embossed surface
KR1020147031190A KR101507294B1 (ko) 2007-04-29 2008-04-25 엠보싱 표면을 갖는 다층 폴리머 중간층의 제조방법
PCT/US2008/061688 WO2008134594A1 (en) 2007-04-29 2008-04-25 Multiple layer polymer interlayers having an embossed surface
BRPI0810998-2A2A BRPI0810998A2 (pt) 2007-04-29 2008-04-25 Intercamada de polímero, método de produzir uma intercamada de polímero e painel vidrado de camadas múltiplas
US12/509,107 US7883761B2 (en) 2007-04-29 2009-07-24 Multiple layer polymer interlayers having an embossed surface
NO20093092A NO20093092L (no) 2007-04-29 2009-10-02 Flerskiktspolymer mellomskikt som har en preget overflate
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US20090286046A1 (en) 2009-11-19
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CA2682529C (en) 2015-06-09
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MX2009011660A (es) 2009-11-10
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CN101668630B (zh) 2014-12-10
RU2469864C2 (ru) 2012-12-20
RU2009136518A (ru) 2011-06-10
JP2010524843A (ja) 2010-07-22
BRPI0810998A2 (pt) 2015-01-27
KR101507294B1 (ko) 2015-03-30
IL201761A0 (en) 2010-06-16
AU2008245544A1 (en) 2008-11-06
CN103921509B (zh) 2016-08-24
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KR20140141720A (ko) 2014-12-10
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NO20093092L (no) 2010-01-28

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