WO2009039053A1 - Procédé de fabrication d'un laminé de verre - Google Patents

Procédé de fabrication d'un laminé de verre Download PDF

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Publication number
WO2009039053A1
WO2009039053A1 PCT/US2008/076349 US2008076349W WO2009039053A1 WO 2009039053 A1 WO2009039053 A1 WO 2009039053A1 US 2008076349 W US2008076349 W US 2008076349W WO 2009039053 A1 WO2009039053 A1 WO 2009039053A1
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WO
WIPO (PCT)
Prior art keywords
vacuum
laminate
assembly
sub
glass
Prior art date
Application number
PCT/US2008/076349
Other languages
English (en)
Inventor
Luc A. Moeyersons
Original Assignee
E. I. Du Pont De Nemours And Company
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from US11/856,385 external-priority patent/US8097113B2/en
Priority claimed from US11/856,531 external-priority patent/US8097114B2/en
Application filed by E. I. Du Pont De Nemours And Company filed Critical E. I. Du Pont De Nemours And Company
Priority to EP08832091A priority Critical patent/EP2190663A1/fr
Publication of WO2009039053A1 publication Critical patent/WO2009039053A1/fr
Priority to ZA2010/00713A priority patent/ZA201000713B/en

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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
    • 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
    • B32B17/10009—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 number, the constitution or treatment of glass sheets
    • B32B17/10036—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 number, the constitution or treatment of glass sheets comprising two outer glass sheets
    • 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
    • B32B17/10743—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 acrylate (co)polymers or salts thereof
    • 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
    • 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
    • B32B17/10807—Making laminated safety glass or glazing; Apparatus therefor
    • B32B17/10816—Making laminated safety glass or glazing; Apparatus therefor by pressing
    • B32B17/10825—Isostatic pressing, i.e. using non rigid pressure-exerting members against rigid parts
    • B32B17/10834—Isostatic pressing, i.e. using non rigid pressure-exerting members against rigid parts using a fluid
    • 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
    • B32B17/10807—Making laminated safety glass or glazing; Apparatus therefor
    • B32B17/10816—Making laminated safety glass or glazing; Apparatus therefor by pressing
    • B32B17/10871—Making laminated safety glass or glazing; Apparatus therefor by pressing in combination with particular heat treatment
    • 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
    • B32B17/10807—Making laminated safety glass or glazing; Apparatus therefor
    • B32B17/10972—Degassing during the lamination
    • 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
    • B32B17/10807—Making laminated safety glass or glazing; Apparatus therefor
    • B32B17/1099—After-treatment of the layered product, e.g. cooling

Definitions

  • This invention relates to laminated safety glass comprising ionomehc or polyvinyl acetal) materials as an interlayer.
  • Laminated glass is utilized in a broad spectrum of products including safety glass found in automobile windshields, windows in trains, airplanes, ships, and can be found in some form in virtually all transportation machinery.
  • Safety glass is characterized by high impact and penetration resistance and does not scatter glass shards and debris when shattered.
  • Laminated glass typically consists of a sandwich of two glass sheets or panels bonded together with an interlayer of a polymeric film or sheet, which is placed between the two glass sheets.
  • One or both of the glass sheets may be replaced with optically clear rigid polymeric sheets, such as sheets of polycarbonate materials.
  • Laminated articles have further evolved to include multiple layers of glass and polymeric sheets bonded together with interlayers of polymeric films or sheets.
  • the interlayer utilized is typically a relatively thick polymer sheet which is well known for it's durability, as well as its to bond effectively to glass, thus creating a far safer product in the event of a crack or crash.
  • these polymeric interlayers possess a combination of characteristics including very high optical clarity, low haze, high impact resistance, high penetration resistance, excellent ultraviolet light resistance, good long term thermal stability, excellent adhesion to glass and other rigid polymeric sheets, low ultraviolet light transmittance, low moisture absorption, high moisture resistance, and excellent long term weatherability, among other requirements.
  • Laminated articles are most commonly formed by subjecting the assembly to elevated temperatures and pressures in an autoclave to bond the components.
  • Non-autoclave processes are generally considered to be less robust, and have a greater yield loss associated with adhesion and lamination failures in the finished article.
  • Fabricators must exercise greater care at process control parameters to achieve the desired adhesion levels and clarity for the finished article. Trapped voids of air and moisture between the layers of the laminate are most often to blame for the defects in the finished laminate. However, even with the most stringent attention to details, lamination integrity failures and cosmetic defects (edge bubbles) may still occur with regularity and without sufficient understanding of the cause.
  • a process that can be used, for example, for preparing a rigid laminate containing a polymer interlayer without use of an autoclave comprising sequentially: providing a rigid layer and polymer interlayer; constructing a sub-assembly comprising the rigid layer and the polymer interlayer; placing the sub-assembly in a vacuum bag or vacuum press; applying a vacuum to the vacuum bag or vacuum press for a maximum of 30 to 60 minutes while maintaining the sub-assembly at a temperature between 10 0 C and 22°C to produce a cooled sub-assembly; increasing the temperature of the cooled sub-assembly to at least 100 0 C or 135°C over a minimum of 10 minutes or 20 minutes to produce a heated sub- assembly; maintaining the heated sub-assembly at minimum of 100 0 C or 135°C for a minimum of 10 minutes or 20 minutes to form a laminate; cooling the laminate at a rate of at least 0.5°C/minute until the laminate reaches
  • FIG. 1 is a time/temperature/pressure cycle plot of representative process conditions used in an illustrative laminate article made with a poly(butyl acetate) interlayer (PVB) and an ionomer interlayer.
  • PVB poly(butyl acetate) interlayer
  • (meth)acrylic as used herein, alone or in combined form, such as “(meth)acrylate”, refers to acrylic and/or methacrylic, for example, acrylic acid and/or methacrylic acid, or alkyl acrylate and/or alkyl methacrylate.
  • This invention is directed to the improvements of a non-autoclave process for making glass laminated articles containing a polymer sheet as a polymeric interlayer. lonomers are well known and the preferred material for making laminated safety glass that exhibit high strength properties.
  • the ionomer useful for the laminate interlayer may have a modulus between 20,000 psi (138 MPa) and 100,000 psi (690 MPa), preferably with a modulus between about 25,000 psi (173 MPa) and about 90,000 psi
  • the ionomer preferably comprises ethylene copolymers that incorporate acid functionality.
  • the ethylene copolymers incorporate from between about 0.1 weight % to about 30 weight % acrylic acids, preferably from about 10 weight % to about 25 weight % acrylic acids, and more preferably from about 15 weight % to about 25 weight % acrylic acids, based on the total weight of the polymer.
  • Acrylic acids include, but are not limited to, acrylic acid, methacrylic acid, itaconic acid, maleic acid, maleic anhydride, fumaric acid, monomethyl maleic acid, and mixtures thereof and most preferably are selected from the group consisting of acrylic acid, methacrylic acid, and mixtures thereof.
  • Ethylene copolymers may optionally further comprise other unsaturated comonomers such as acrylates and methacrylates.
  • the other unsaturated comonomers may be selected from the group consisting of methyl acrylate, methyl methacrylate, butyl acrylate, butyl methacrylate, glycidyl methacrylate, vinyl acetate, and mixtures thereof.
  • the ethylene copolymers used in the polymeric sheets may comprise between 0 and about 50 weight percent of the other unsaturated comonomer, based on the total weight of the ethylene copolymer composition.
  • the ethylene copolymers may preferably incorporate between 0 and about 25 weight percent of the other unsaturated comonomer and may most preferably incorporate between 0 weight percent and about 10 weight percent of the other unsaturated comonomer.
  • the ethylene copolymers can be neutralized from 0 to about 100 percent with metallic ions based on the total carboxylic acid content.
  • the ethylene copolymers maybe neutralized from about 10 to about 90 percent, more preferably maybe neutralized about 20 to about 80 percent.
  • the metallic ions used may be monovalent, divalent, trivalent, multivalent, or mixtures thereof such as sodium, potassium, lithium, silver, mercury, zinc, copper, or mixtures of two or more thereof. Examples of such polymer include Surlyn ® available from DuPont.
  • Suitable ionomer sheets are available commercially from DuPont as Sentryglas ® Plus sheeting.
  • Polyvinyl acetal is a thermoplastic resin derived by the condensation of an aldehyde with polyvinyl alcohol and can include polyoxymethylene, polyoxyethylene, polyoxypropylene, polyoxypolybutylene, or combinations of two or more thereof.
  • Polyoxybutylene also known as polyvinyl butyral) (PVB)
  • PVB polyvinyl butyral
  • Suitable polymeric sheets are available commercially.
  • Plasticized poly (vinyl butyral) sheet is commercially available from DuPont as BUTACITE ® PVB resin sheeting.
  • the polymer sheet may comprise poly (vinyl acetal) having an average molecular weight range of from about 30,000 to about 600,000, preferably from about 45,000 to about 300,000, more preferably from about 200,000 to 300,000 Daltons, as measured by size exclusion chromatography using low angle laser light scattering. More preferred is a poly (vinyl butyral) material comprising, on a weight basis, about 5 to about 30 %, preferably about 11 to about 25 %, and more preferably about 15 to about 22 %, hydroxyl groups calculated as polyvinyl alcohol.
  • a preferred polyvinyl acetal) material comprises 0 to about 10 %, preferably 0 to about 3 % residual ester groups, calculated as polyvinyl ester, typically acetate groups, with the balance being butyraldehyde acetal.
  • the PVB material may further comprise a minor amount of acetal groups other than butyral, for example, 2-ethyl hexanal, as disclosed in US5137954.
  • polyvinyl acetal further comprises a plasticizer.
  • the amount of plasticizer depends on the specific polyvinyl acetal) resin and the properties desired for the laminate.
  • plasticizers which can be used are known in the art, for example, as disclosed in US Patents
  • Plasticizers commonly employed are esters of a polybasic acid or a polyhydric alcohol.
  • Preferred plasticizers are triethylene glycol di-(2-ethyl butyrate), triethylene glycol di-2- ethylhexanoate, triethylene glycol di-n-heptanoate, oligoethylene glycol di- 2-ethylhexanoate, tetraethylene glycol di-n-heptanoate, dihexyl adipate, dioctyl adipate, mixtures of heptyl and nonyl adipates, dibutyl sebacate, thbutoxyethylphosphate, isodecylphenylphosphate, triisopropylphosphite, polymeric plasticizers such as the oil-modified sebacid alkyds, and mixtures of phosphates and adipates, and adipates and alkyl benzyl phthalates. Generally between about 15 to about 80 parts of plasticizer per hundred parts of resin, preferably about 25 to about 45 parts of plasticizer per hundred
  • a plasticized polyvinyl acetal) composition for use in the interlayer of the multilayer laminates may be formed by initially mixing polyvinyl acetal) resin with plasticizer (and optionally other additives, such as described above for the coating matrix material), and then extruding the formulation through a sheet-shaping die, i.e. forcing molten, plasticized polyvinyl acetal) through a horizontally long, vertically narrow die opening substantially conforming in length and width to that of the sheet being formed.
  • Rough surfaces on one or both sides of the extruding sheet are provided by the design of the die opening and the temperature of the die exit surfaces through which the extrudate passes, as disclosed in, for example, US4281980.
  • Alternative techniques for producing a rough surface on an extruding poly (vinyl butyral) sheet involve the specification and control of one or more of polymer molecular weight distribution, water content and melt temperature. Such techniques are disclosed in
  • the extruded sheet may be passed over a specially prepared surface of a die roll positioned in close proximity to the exit of the die which imparts the desired surface characteristics to one side of the molten polymer.
  • a specially prepared surface of a die roll positioned in close proximity to the exit of the die which imparts the desired surface characteristics to one side of the molten polymer.
  • the polymeric interlayer has a thickness of about 10 mils (0.25 mm), or greater.
  • the polymer sheet may have a thickness of about 15 mils (0.38 mm), or greater, based on enhanced penetration strength of the laminates produced therefrom. More preferably, the polymer sheet may have a thickness of about 30 mils (0.75 mm), or greater, based on further enhanced penetration strength of the laminates produced therefrom.
  • the polymeric sheet may have a thickness of about 50 mils (1.25 mm), or greater, based on even further enhanced penetration strength of the laminates produced therefrom.
  • the enhanced penetration strength is necessary to satisfy many of the current mandated requirements for hurricane and threat resistance.
  • Many end-uses in the current environment require the ethylene copolymer interlayer to be even thicker, lnterlayers thicker than 60 mils (1.50 mm), 90 mils (2.25 mm), and even thicker than 120 mils (3.00 mm), are becoming common in the marketplace.
  • Suitable polymeric sheets may be formed by any suitable process, such as extrusion, calendering, solution casting or injection molding.
  • the polymer sheet is preferably formed by extrusion. Extrusion is particularly preferred for formation of "endless" products, such as films and sheets, which emerge as a continuous length.
  • the polymeric film useful in the multilayer laminate articles may be formed from any polymeric matrix material.
  • the polymeric film is a biaxially oriented poly(ethylene terephthalate) film, a cellulose acetate film or a polycarbonate film.
  • one or both surfaces of the polymeric film may be treated to enhance the adhesion to the coating or to the polymeric sheet or both.
  • This treatment may take any form known within the art, including adhesives, primers, such as silanes, flame treatments, plasma treatments, electron beam treatments, oxidation treatments, corona discharge treatments, chemical treatments, chromic acid treatments, hot air treatments, ozone treatments, ultraviolet light treatments, sand blast treatments, solvent treatments, and the like and combinations thereof.
  • a film has a thickness of about 10 mils (0.25 mm) or less, between about 0.5 mils (0.012 millimeters (mm)), to about 10 mils (0.25 mm), or about 1 mil (0.025mm) to about 5 mils (0.13mm).
  • a sheeting calender For manufacturing large quantities of sheets, a sheeting calender is employed.
  • the rough film is fed into the gap of the calender, a machine comprising a number of heatable parallel cylindrical rollers which rotate in opposite directions and spread out the polymer and stretch it to the required thickness.
  • the last roller smoothes the sheet thus produced.
  • the final roller If the sheet is required to have a textured surface, the final roller is provided with an appropriate embossing pattern.
  • the sheet may be reheated and then passed through an embossing calender.
  • the calender is followed by one or more cooling drums. Finally, the finished sheet is reeled up or cut into lengths and stacked.
  • the polymeric sheet may have a smooth surface.
  • the polymeric sheet to be used as an interlayer within laminates may have a roughened surface to effectively allow most of the air to be removed from between the surfaces of the laminate during the lamination process. This may be accomplished, for example, by mechanically embossing the sheet after extrusion, as described above, or by melt fracture during extrusion of the sheet and the like.
  • the as extruded sheet may be passed over a specially prepared surface of a die roll positioned in close proximity to the exit of the die which imparts the desired surface characteristics to one side of the molten polymer.
  • sheet formed of polymer cast thereon may have a rough surface on the side which contacts the roll which generally conforms respectively to the valleys and peaks of the roll surface.
  • This rough surface is only temporary and particularly functions to facilitate deaihng during laminating after which it is melted smooth from the elevated temperature from the non-autoclave processes.
  • Biaxially stretched polymeric sheets are preferred.
  • Adhesives and primers may be used to enhance the bond strength between the laminate layers, if desired, as is generally known in the art.
  • silane coupling agents may be applied to the films and sheets to enhance the adhesion between layers.
  • Specific examples of useful silane coupling agents are gammaglycidoxypropylthmethoxysilane or gamma-aminopropyltriethoxysilane.
  • said silane coupling agents are added at a level of about 0.01 to about 5 weight percent based on the total weight of the film or sheet composition.
  • An example of a preferred primer is polyallyl amine.
  • adhesives are epoxy and siloxane resins.
  • ionomehc composition may also be added to ionomehc composition.
  • additives including but not limited to antioxidants, ultraviolet absorbers, ultraviolet stabilizers, thermal stabilizers, and colorants, may also be added to ionomehc composition. See, e.g., US5190826.
  • the extruded sheet may be passed over a specially prepared surface of a die roll positioned in close proximity to the exit of the die which imparts the desired surface characteristics to one side of the molten polymer.
  • sheet formed of polymer cast thereon may have a rough surface on the side which contacts the roll which generally conforms respectively to the valleys and peaks of the roll surface.
  • Such die rolls are disclosed in, for example, US4035549. As is known, this rough surface is only temporary and particularly functions to facilitate de-airing during laminating after which it is melted smooth from the elevated temperature and pressure associated with autoclaving and other lamination processes.
  • the polymeric sheets may further comprise additives such as thermal stabilizers, ultraviolet (UV) absorbers, UV stabilizers, plasticizers, organic peroxides, processing aides, flow enhancing additives, lubricants, pigments, dyes, flame retardants, impact modifiers, nucleating agents to increase crystallinity, antiblocking agents such as silica, adhesion promoters, dispersants, surfactants, chelating agents, coupling agents, adhesives, primers, or combinations of two or more thereof.
  • additives such as thermal stabilizers, ultraviolet (UV) absorbers, UV stabilizers, plasticizers, organic peroxides, processing aides, flow enhancing additives, lubricants, pigments, dyes, flame retardants, impact modifiers, nucleating agents to increase crystallinity, antiblocking agents such as silica, adhesion promoters, dispersants, surfactants, chelating agents, coupling agents, adhesives, primers, or combinations of two or more thereof.
  • UV absorbers
  • the rigid sheets useful in the laminates may be glass or rigid transparent plastic sheets, such as, for example, polycarbonates, acrylics, polyacrylates, cyclic polyolefins, such as ethylene norbornene polymers, metallocene-catalyzed polystyrenes and the like and combinations thereof.
  • Metal or ceramic plates may also be suitable, if transparency is not required for the laminate.
  • glass is meant to include not only window glass, plate glass, silicate glass, sheet glass, and float glass, but also includes colored glass, specialty glass which includes ingredients to control, for example, solar heating, coated glass with, for example, sputtered metals, such as silver or indium tin oxide, for solar control purposes and other specialty glasses.
  • the type of glass to be selected for a particular laminate depends on the intended use. A typical glass is 90 mil thick annealed flat glass.
  • the polymeric interlayer sheet generally has a moisture content of about 0.2 wt.%, and typical commercial autoclave grades are about 0.3 to 0.6 wt.%, prior to being plied into the laminated article sub-assembly.
  • a manufacturer of laminates may store the polymeric interlayer at about 6°C and 20 0 C, and 20 and 40 percent relative humidity for at least 24 hours prior to use. The manufacturer of laminates may then take the polymeric sheet out of the controlled storage conditions and ply up the laminated assembly in ambient temperature and humidity conditions.
  • FIG. 1 is plot of both temperature and vacuum pressure against a time scale as the components proceed through the process to form a laminate in the non-autoclave process.
  • the temperatures shown in FIG. 1 are understood to be the temperature of component layers that ultimately are formed into the laminate article, and not necessarily the environment around the component layers.
  • This invention provides a more optimal lamination by conditions for storing the polymer interlayer and rigid glass layers prior to assembling into the sub-assembly, as well as assembling the sub-assembly in controlled temperature conditions.
  • All layers of the laminated article including the polymeric interlayer and the rigid glass sheets, is conditioned and allowed to equilibrate at about 10 0 C to about 23°C as well as less than about 40 percent relative humidity prior to assembly into the sub-assembly (FIG. 1 , 1). All layers of the laminated article may be conditioned and allowed to equilibrate at about 10 0 C and less than 18°C as well as less than 40 percent relative humidity prior to assembly. Any technique may be used to achieve these temperature conditions, but most commonly the temperature may be controlled by air conditioning.
  • the polymer interlayer sheet is positioned between two rigid layers, such as two glass plates, to form a glass/interlayer/glass sandwich assembly.
  • the laminated article at this stage is referred to as a sub-assembly (FIG 1 , 2).
  • the sub-assembly may be constructed as a sandwich structure. All surfaces of the glass layer may be clean and dried prior to use in making the sub-assembly.
  • the component layers (glass layer/interlayer/second glass layer) may be applied sequential in layers to make the sub-assembly at about 10 0 C and less than 23°C as well as less than 40 percent relative humidity.
  • the sub-assembly may be constructed at about 10 0 C and less than 18°C as well as less than 40 percent relative humidity. Once assembled in the controlled temperature and humidity conditions, the sub-assembly may be stored at these conditions prior to lamination or may immediately be processed. Any technique may be used to achieve these temperature and humidity conditions, but most commonly the temperature may be controlled by air conditioning. If the environment is typically greater than 40 percent relative humidity, dehumidifying equipment or sieve air dryers for a storage air may be useful.
  • a glass sheet, an interlayer composed of a polymeric sheet, and a second glass sheet are laminated together under heat and the assembly held under a vacuum (for example, in the range of about 90 kPa to 100 kPa), to remove air or de-airing of the laminating sub-assembly.
  • the sub-assembly is placed into a bag capable of sustaining a vacuum ("a vacuum bag").
  • the air is drawn out of the vacuum bag using a vacuum line or other means of pulling a vacuum on the vacuum bag.
  • the vacuum bag is sealed while maintaining the vacuum.
  • the de-airing of the sub-assembly can be improved if the vacuum pressure is applied to a chilled sub-assembly structure (FIG.
  • One embodiment is applying the vacuum to the sub-assembly while the temperature of the sub-assembly is kept at about 10 0 C and less than about 23°C.
  • Preferred is applying the vacuum pressure to the sub- assembly while the temperature of the sub-assembly is kept at about 10 0 C and less than about 18°C. Any technique may be used to achieve these temperature conditions, but most commonly the temperature may be controlled by air conditioning. As practical, maximum vacuum pressure may be applied to maximize air removal since superatmospheric pressure (from the autoclave) is unavailable to assist in dissolving residual air in the sheet during bonding to the glass.
  • the assembly is subject to this vacuum without heating over a brief period during which the rough surface on the PVB sheet is intact to facilitate air removal. This period varies with the design of the system used and is typically about 10 to about 30 minutes. The absence of heat during this phase avoids premature sealing of the sheet to the glass during air removal.
  • the chilling of all layers as well as fabricating the sub-assembly in controlled temperature and humidity conditions help ensure that the surface roughness of the polymeric sheet retain a higher modulus longer, and allow a more uniform and overall greater degree of evacuation of any air that might be trapped between the layers of the sub-assembly. This is essential to the improving the uniformity of the laminate properties produced by the non-autoclave lamination process.
  • polymeric interlayer sheets will have geometrically regular or irregular (random) patterns on its surfaces to help facilitate deairing.
  • the surface patterns provide grooves or channels on both surface faces, which are defined by minute collapsible projections. During deairing, air at the interface with a glass layer is conventionally channeled through these grooves out through the periphery of the assembly.
  • the projections are an integral part of the interlayer sheet which melt and collapse during heating after air removal.
  • the polymeric interlayer may provide a clear, smooth, void-free surface which can be bonded to the abutting transparent glass layer.
  • the edges are enclosed in a sealed space.
  • One way to accomplish this is to insert the sub- assembly in a flexible rubber or nylon bag having a port communicating with a vacuum source (FIG. 1 , 3).
  • a ring in communication with a vacuum source seals around the edges only of the assembly.
  • a breather layer is used between the flexible bag and the laminate assembly enclosed therein. Such breather layer resists the flexible bag being prematurely tightly drawn down around the edges of the enclosed assembly when vacuum is imposed on the interior of the bag before all air from inside is evacuated.
  • the sub-assembly may be placed in either the vacuum bag or the vacuum ring may be applied to the sub-assembly and evacuated at about 10 0 C and about less than 23°C.
  • the sub-assembly may be placed in either the vacuum bag or the vacuum ring may be applied to the sub- assembly and evacuated at about 10 0 C and about 18°C ambient conditions. After enclosing the edges in a sealed space, vacuum is drawn on the sealed space to remove air therefrom and evacuate moisture and air from the sub-assembly.
  • the laminate assembly while maintaining vacuum is gradually heated to a temperature sufficient to seal the edges of the glass layers to the encapsulated polymer interlayer (FIG. 1 , 4).
  • Any means may be used to efficiently heat the laminate subassembly while under vacuum.
  • Conventional ovens with variety of heating sources, such as gas-fired or electrical resistivity may be used; or continuous oven with infra-red sources, may be utilized as long as the vacuum may be adequately maintained about sub-assembly.
  • the onset of the sealing may occur with the polymer interlayer at as low as 27°C, but in order to achieve uniform sealing around the complete sub-assembly, the temperature may reach about 95°C and happens about 20 minutes into the heating cycle in the embodiment encompassed by the plot displayed in Figure 1.
  • the temperature of the assembly is further increased to about 125°C to about 135°C while maintaining the vacuum on the process.
  • This increase in temperature may be desirable to obtain mature edge seal for a minimum of 20 minutes, and assure that all layers of the sub-assembly have sufficiently adhered together (FIG. 1 , 5).
  • Controlled cooling and release of the vacuum may be desired to prevent the formation of edge bubbles of the laminate as well as optical transparency in the polymer laminate.
  • the temperature of the process is gradually lowered at a rate of about 0.5°C/minute to about 5°C/minute. It is desirable to continue to maintain the vacuum until the laminate article cools to about 40 0 C (FIG. 1 , 6). Rapid cooling of the laminate structure prevents finely dispersed crystallites from being formed and thereby, creating a hazy interlayer. Rapid quenching of the thick layers can help the laminate have the desired transparency of the glass laminate.
  • the vacuum may also be gradually reduced over about 10 minutes up to the time necessary for the laminate article reaches 40 0 C.
  • edge bubbles may form in the laminate article.
  • Conditions for the cooling and vacuum removal may vary with the complexity of the laminated structure and the means used to heat and cool the process. Maintaining the vacuum until the laminate cools to 40°C is preferred to promote good optical qualities and bubble free edges.
  • the laminate can then be removed from the vacuum bag or ring after further cooling to ambient temperature (FIG 1 , 7).
  • apparatus which includes a programmable oven or a conveyor for the subassembly to sequentially pass through zones maintained at the desired temperatures, but at such a rate that the heating of the laminate article is most economically achieved
  • vacuum and temperature profile of the process may vary from that shown in FIG 1 depending, for example, on the capacity and layout of the process equipment.
  • the laminate articles may include additional layers, such as other polymeric sheets, other coated or uncoated polymeric films.
  • Each sub-assembly had a vacuum deairing ring applied around its peripheral edges and the de-airing ring was connected to a vacuum source.
  • the vacuum source applied 95 kPa to the sub-assembly while it was maintained at 15.5°C for 30 minutes.
  • the all sub-assemblies and deairing rings were loaded vertically (with the short edge on the bottom) into three carts, so as to position approximately 50 mm between each sub-assembly.
  • the spacing of the laminates desirably allows for hot air to flow thoroughly around each sub-assembly while in the oven.
  • the carts were positioned into a 2500 mm wide, 3500 mm high and 3500 mm deep electrical circulating air convention oven, which was heated to 135°C.
  • the surface temperature of the sub-assemblies was monitored by an infrared thermometer during the heating stage to verify that the sub-assemblies were reaching the proper temperature.
  • Each sub-assembly remained under vacuum while in the oven.
  • the sub-assembly reached the targeted 135°C temperature over a 50 minute time period. Vacuum was continued to be applied while the sub- assemblies were held in the oven for an additional 40 minutes to ensure that the glass, interlayer, and glass firmly adhered to each other. At the conclusion of the heating cycle, the vacuum pump and oven heating were turned off. However, the vacuum remained at the approximately the same levels on the laminated structure because of the integrity of the vacuum system did not appreciably bleed down the vacuum. The carts containing the 60 laminate articles remained in the oven overnight to cool. The de-airing vacuum ring was disconnected from the vacuum source, once the laminate structure was verified to be below 40 0 C.
  • the laminated structure was removed from the de-airing ring. All sixty laminated structures were visually inspected. Each laminate was found to have high optical clarity, indicating that the process had been effective at removing the air and moisture from between the layers and that the layers had adhered securely to each other. In addition, all sixty of the laminate structures where found to be clear visual clarity and free of edge bubbles.

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  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Joining Of Glass To Other Materials (AREA)

Abstract

L'invention porte sur un procédé sans autoclave pour fabriquer un laminé de verre, comprenant l'application sous vide d'un sous-ensemble, comprenant une couche rigide et une couche intermédiaire polymère, dans un sac à vide ou une presse sous vide, suivi par un chauffage, un refroidissement et une libération du vide.
PCT/US2008/076349 2007-09-17 2008-09-15 Procédé de fabrication d'un laminé de verre WO2009039053A1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
EP08832091A EP2190663A1 (fr) 2007-09-17 2008-09-15 Procédé de fabrication d'un laminé de verre
ZA2010/00713A ZA201000713B (en) 2007-09-17 2010-01-29 Process for the manufacture of a glass laminate

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US11/856,385 2007-09-17
US11/856,385 US8097113B2 (en) 2007-09-17 2007-09-17 Glass laminate containing poly vinyl acetal
US11/856,531 US8097114B2 (en) 2007-09-17 2007-09-17 Glass laminate containing ionomer
US11/856,531 2007-09-17

Publications (1)

Publication Number Publication Date
WO2009039053A1 true WO2009039053A1 (fr) 2009-03-26

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WO (1) WO2009039053A1 (fr)
ZA (1) ZA201000713B (fr)

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Publication number Priority date Publication date Assignee Title
EP2298707A1 (fr) * 2008-06-16 2011-03-23 Central Glass Company, Limited Procédé de fabrication de verre feuilleté intercalé avec un film plastique et verre feuilleté intercalé avec un film plastique
WO2013017797A1 (fr) * 2011-08-04 2013-02-07 Saint-Gobain Glass France Procédé de fabrication d'un vitrage a effet decoratif
CN109733045A (zh) * 2019-01-08 2019-05-10 江苏铁锚玻璃股份有限公司 夹层玻璃热压方法及其热压装置
FR3081768A1 (fr) 2018-06-04 2019-12-06 Sunpartner Technologies Procede d'assemblage de modules d'epaisseur differentes en vue de leur integration dans un produit verrier
IT201800021127A1 (it) 2018-12-27 2020-06-27 Antonio Mazzaroppi Metodo di laminazione del vetro senza sbordatura del materiale plastico
WO2021254977A1 (fr) 2020-06-17 2021-12-23 Saint-Gobain Glass France Procédé de satrification d'une vitre composite sans un autoclave

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US5147485A (en) * 1990-10-29 1992-09-15 Ford Motor Company Lamination of semi-rigid material between glass
US5536347A (en) * 1994-09-22 1996-07-16 Monsanto Company No autoclave process for forming a safety glass laminate
EP0748687A2 (fr) * 1995-06-16 1996-12-18 Ppg Industries, Inc. Procédé de fabrication d'un laminé de verre et plastique
US20060141212A1 (en) * 2000-10-26 2006-06-29 Smith Charles A Interlayers for laminated safety glass with superior de-airing and laminating properties and process for making the same
US20060182983A1 (en) * 2004-10-29 2006-08-17 Paul John W Thermoplastic resin compositions suitable for use in transparent laminates

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5147485A (en) * 1990-10-29 1992-09-15 Ford Motor Company Lamination of semi-rigid material between glass
US5536347A (en) * 1994-09-22 1996-07-16 Monsanto Company No autoclave process for forming a safety glass laminate
EP0748687A2 (fr) * 1995-06-16 1996-12-18 Ppg Industries, Inc. Procédé de fabrication d'un laminé de verre et plastique
US20060141212A1 (en) * 2000-10-26 2006-06-29 Smith Charles A Interlayers for laminated safety glass with superior de-airing and laminating properties and process for making the same
US20060182983A1 (en) * 2004-10-29 2006-08-17 Paul John W Thermoplastic resin compositions suitable for use in transparent laminates

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2298707A1 (fr) * 2008-06-16 2011-03-23 Central Glass Company, Limited Procédé de fabrication de verre feuilleté intercalé avec un film plastique et verre feuilleté intercalé avec un film plastique
EP2298707A4 (fr) * 2008-06-16 2013-02-27 Central Glass Co Ltd Procédé de fabrication de verre feuilleté intercalé avec un film plastique et verre feuilleté intercalé avec un film plastique
WO2013017797A1 (fr) * 2011-08-04 2013-02-07 Saint-Gobain Glass France Procédé de fabrication d'un vitrage a effet decoratif
FR2978698A1 (fr) * 2011-08-04 2013-02-08 Saint Gobain Vitrage a effet decoratif
EP2821224A1 (fr) * 2011-08-04 2015-01-07 Saint-Gobain Glass France Procédé de fabrication d'un vitrage à éffet décoratif
EP2739472B1 (fr) 2011-08-04 2019-02-27 Saint-Gobain Glass France Procédé de fabrication d'un vitrage a effet decoratif
FR3081768A1 (fr) 2018-06-04 2019-12-06 Sunpartner Technologies Procede d'assemblage de modules d'epaisseur differentes en vue de leur integration dans un produit verrier
IT201800021127A1 (it) 2018-12-27 2020-06-27 Antonio Mazzaroppi Metodo di laminazione del vetro senza sbordatura del materiale plastico
CN109733045A (zh) * 2019-01-08 2019-05-10 江苏铁锚玻璃股份有限公司 夹层玻璃热压方法及其热压装置
CN109733045B (zh) * 2019-01-08 2023-08-25 江苏铁锚玻璃股份有限公司 夹层玻璃热压方法及其热压装置
WO2021254977A1 (fr) 2020-06-17 2021-12-23 Saint-Gobain Glass France Procédé de satrification d'une vitre composite sans un autoclave

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EP2190663A1 (fr) 2010-06-02
ZA201000713B (en) 2011-04-28

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