EP1268189A4 - Flammbeständige optische filme - Google Patents
Flammbeständige optische filmeInfo
- Publication number
- EP1268189A4 EP1268189A4 EP01916187A EP01916187A EP1268189A4 EP 1268189 A4 EP1268189 A4 EP 1268189A4 EP 01916187 A EP01916187 A EP 01916187A EP 01916187 A EP01916187 A EP 01916187A EP 1268189 A4 EP1268189 A4 EP 1268189A4
- Authority
- EP
- European Patent Office
- Prior art keywords
- flame retardant
- pet
- film structure
- sheet
- coating
- Prior art date
- Legal status (The legal status 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 status listed.)
- Withdrawn
Links
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/075—Silicon-containing compounds
- G03F7/0755—Non-macromolecular compounds containing Si-O, Si-C or Si-N bonds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B15/00—Layered products comprising a layer of metal
- B32B15/04—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B15/08—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- 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
- B32B27/36—Layered products comprising a layer of synthetic resin comprising polyesters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
- C08L63/10—Epoxy resins modified by unsaturated compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
- C09J175/04—Polyurethanes
- C09J175/06—Polyurethanes from polyesters
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K21/00—Fireproofing materials
- C09K21/14—Macromolecular materials
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/0005—Production of optical devices or components in so far as characterised by the lithographic processes or materials used therefor
- G03F7/001—Phase modulating patterns, e.g. refractive index patterns
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/0042—Photosensitive materials with inorganic or organometallic light-sensitive compounds not otherwise provided for, e.g. inorganic resists
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/0045—Photosensitive materials with organic non-macromolecular light-sensitive compounds not otherwise provided for, e.g. dissolution inhibitors
Definitions
- the present invention pertains to the field of sheets or films especially solar control films and solar control window shades made from such films which are susceptible to burning. More particularly, the present invention pertains to flame retardant films or sheets such as solar control films and solar control window shades made from such films which have desirable flame retardant characteristics without sacrificing the optical clarity and visible light transmission characteristics which are desired in this field of technology. The present invention also pertains to the field of compositions which can be used to form flame retardant adhesive layers and flame retardant optical layers in sheets or films especially solar control film structures and solar control window shades made from such film structures.
- Polymeric materials are combustible and will easily burn when subjected to sufficient heat, e.g. , flame, in an oxidizing environment.
- the dynamics of polymer degradation are intensified when polymer materials are in a thin film structure.
- Solar control window shades are typically made from flexible transparent film or sheet material which includes one or more layers of optical coatings which are designed to block or reflect certain portions of the electromagnetic spectrum.
- solar control window shades are typically designed to block or reflect infrared and/or ultraviolet light and reduce the amount of visible light which passes therethrough while maintaining some degree of visible light transmittance. It is particularly desirable in many applications to provide a solar control window shade which has the desired the blocking and/or reflecting characteristics while maintaining good optical clarity and visible light transmittance.
- the combustibility of such window shades have become of great concern recently since such window shades are typically used indoors where they can become a fire hazard. In this regard some countries have set flame retardant criteria for such solar control window shades and the like.
- Solar control window shades are generally made from a flexible transparent film structure which includes one or more layers of polyethylene terephthalate (PET). Generally an adhesive is used to bond together the PET films which are used to make the solar control window shade. In addition, the solar control window shade will also include one or more layers of coatings which are formulated and applied to provide the desired light blocking and/or reflecting characteristics.
- PET polyethylene terephthalate
- the solar control window shade will also include one or more layers of coatings which are formulated and applied to provide the desired light blocking and/or reflecting characteristics.
- the flame retardant materials which are used in this invention are chemically bonded into polymeric materials of the adhesive and coatings, preferably as an integral component of the polymeric material.
- the flame retardant materials used in this invention are nonmigratory, nonplasticizing and do not impede the curing process. Most importantly they do not degrade the desired optical characteristics of the film structure.
- an organic solvent solution which can be used to form a flame retardant, optically clear, thermosetting adhesive layer in the solar control film structure.
- the solution comprises adhesive precursor compounds dissolved in an organic solvent.
- the adhesive precursors are isocyanate terminated polyester urethane and tetrabromobisphenol A.
- the organic solution containing the adhesive precursors dissolved therein can be applied as a thin coating on a thin flexible sheet which is used to make the solar control film structure of the present invention.
- the sheet may be PET or any other flexible transparent polymeric sheet material which is conventionally used to manufacture solar control film structures.
- the coating is then allowed to cure (thermoset) in a reaction in which the tetrabromobisphenol A reacts with the isocyanate terminated polyester urethane. Curing and evaporation of the organic solvent forms the desired flame retardant adhesive layer.
- an organic solvent solution which can be used to form the optical coatings in the solar control film structure.
- the organic solution which is used to produce the flame retardant optical coating contains organic solvent in which are dissolved compounds which, upon curing, form a flame retardant aery late coating.
- the flame retardant acrylate coating is a brominated acrylated epoxy coating.
- Suitable precursors for forming the brominated acrylated epoxy coating are brominated acrylated epoxy oligomer and bis(2-chloroethyl) vinyl phosphonate.
- the organic solution contains brominated acrylated epoxy oligomer and bis(2- chloroethyl) vinyl phosphonate dissolved in the organic solvent. The organic solution is applied to the sheet where it is cured to form the optical coating.
- this invention also provides flame retardant, optically clear composite film structures.
- this invention provides such a film which comprises at least one flexible sheet of transparent polymer such as polyethylene terephthalate (PET) with a flame retardant coating thereon.
- the preferred flame retardant coating is the reaction product of brominated acrylated epoxy oligomer and bis(2-chloroethyl) vinyl phosphonate or bis(B- chloroethyl) vinyl phosphonate.
- the film structure further comprises a flame retardant adhesive layer which is used to bond multiple layers of flexible sheet (e.g. , PET) together.
- the flexible sheet which includes the flame retardant optically clear thermosetting adhesive and/or the flame retardant optical coating may further include any conventional solar control element which has an effect on the light transmission and/or reflection characteristics of the film structure.
- the embodiments of this invention which include the flame retardant adhesive layer contain two or more transparent flexible sheets of polymeric material such as PET which are bound together with the flame retardant adhesive.
- Figures 1-7 illustrate the multilayered configurations of various embodiments of the film structures according to the present invention.
- the adhesive layer and optical coating layer used in the present invention does not adversely effect the transmission of visible light through the film structure nor does it hinder the optical clarity of the film structure such as by the development of haze.
- visible light means light in the wavelength range of 400 to 750 nanometers.
- optical clarit refers to film materials with low haze, e.g. , generally less than 25 % haze, more preferably less than 20% haze. Haze in an otherwise potentially optically clear polymeric material typically has the effect of scattering of visible light passing through polymeric materials. Thus, scattered visible light is a useful surrogate measurement for haze. For instance, a film characterized by 25 % haze will exhibit scatter of 25 % of the transmitted visible light In an optically clear polymeric film or composite of polymeric films, optical clarity is further manifest by the ability to distinguish shapes viewed through such films.
- the film structures of this invention may include any conventional solar control element.
- the films of this invention may include various types of coatings, layers and compositions which effect the transmission and/or reflection of light through the film structure.
- the flame resistant solar control film structure of the present invention may include elements which block or reflect at least a portion of the incident infrared, visible or ultraviolet light.
- the film structure has a visible light transmission in the range of 3 to 50% of incident visible light in the wavelength range of 400 to 750 nanometers.
- the film structure of the present invention will have no more than 25 % haze, preferably less than 25 % haze.
- One aspect of the present invention provides organic solvent solutions which are useful for making flame retardant, optically clear, thermosetting adhesive, e.g. , organic solvents which contain adhesive polymer with chemically bonded flame retardant components.
- the preferred chemically bonded flame retardant component is tetrabromobisphenol A.
- a preferred adhesive comprises the reaction product of a polymeric adhesive precursor, e.g. , isocyanate terminated polyester urethane, and tetrabromobisphenol A.
- Another aspect of this invention provides organic solvent solution which is useful for making flame retardant optically clear coating compositions, e.g. , optically clear coatings of brominated acrylated epoxy, with chemically bonded flame retardant components.
- a preferred chemically bonded flame retardant component is bis-(2-chloroethyl) vinyl phosphonate.
- Such components are preferably reacted by UV initiated free radical polymerization reaction, e.g. , by the use of photoinitiators and free radical generators such as peroxides which are well known to those skilled in the art.
- photoinitiators and free radical generators are advantageously included in the organic solution which is used to form the optically clear coating.
- the flame retardant adhesive and coating compositions of this invention are believed to suppress the generation of free radicals.
- the phosphonate containing coating composition supports flame retardation by promoting the formation of a char which tends to occlude oxygen access to a burning surface.
- organic solvents which may be used in this invention for the formation of the aforementioned adhesive and optical coating solvent solutions, include organic solvents such as methyl ethyl ketone (MEK), methyl isobutyl ketone (MIBK), toluene, xylene and dimethylformamide.
- MEK methyl ethyl ketone
- MIBK methyl isobutyl ketone
- toluene xylene and dimethylformamide.
- optically clear films are typically provided as composite laminates comprising two or more optically active polyester films.
- Such optically active polyester films typically comprise polyethylene terephthalate (PET) film, commonly in a thickness of about 25 micrometers (1 mil) to about 100 micrometers (4 mils).
- PET polyethylene terephthalate
- the optical activity of PET film results from the incorporation of light absorbers, e.g. , dyes and UV absorbers, into the PET film, the application of metal coating and/or metal oxide coating on the PET film or a combination of light absorbers and/metal/metal oxide coating.
- Useful metals for optically active coatings on PET films include silver, aluminum, nickel and metal oxides such as indium oxide, tin oxide and the like. Metal and oxide coatings can be in the range of about 10 to 100 nanometers. Metal and/or metal oxide layers can be applied by vacuum deposition methods well known to those skilled in the art of sputtering.
- a useful optically clear, flame retardant, optical film composite of this invention comprises at least one layer of PET coated with a metal layer and adhered to at least one dyed, optically active layer of PET by a flame retardant adhesive, wherein at least one of the layers of PET film is coated with a flame retardant coating.
- the flame retardant optical composites of this invention may be fabricated with sufficient amounts of flame retardant adhesive and coating to provide composites which meet national flame retardant standards such as (a) United Kingdom flame retardant specification BS 5878: Part 2: 1980 (1993) and Test Method BS 5438: 1976, and/or (b) German Test Method DIN 41021.
- the flame retardant adhesive compositions and flame retardant coating compositions of this invention can be applied to PET film by any of a variety of methods known to those skilled in the art of film coating and composite film manufacture. Preferred methods include gravure coating and slot die coating.
- FIGS 1-7 illustrate various embodiments of the multilayered flame retardant film structures in accordance with the present invention.
- Figure 1 illustrates an embodiment of one of the multilayered or composite film structures according to the present invention.
- the embodiment illustrated in figure 1 includes PET sheet 1 which has a coating 2 thereon.
- Coating 2 is a flame retardant optically clear coating (optical coating) of the present invention.
- coating 2 comprises the reaction product of brominated acrylated epoxy oligomer and bis(2-chloroethyl) vinyl phosphonate.
- FIG 2 illustrates an embodiment of the invention wherein PET film or sheet 1 includes a metal layer coating 3 thereon.
- the metal layer 3 may be any of the conventional metal layers known to those skilled in the art which alter the optical characteristics of the PET film.
- the metal layer may be selected for altering the transmission of light through the PET film or for providing desired reflection or antireflection characteristics.
- Any of the metal coatings used in the present invention may be selected to achieve the above- noted light transmission and/or light reflection or antireflection characteristics.
- the embodiment in figure 2 also includes flame retardant optical coating 2 which is applied onto the metal coated PET sheet.
- FIG. 1 illustrates an embodiment of the invention wherein PET sheet 1 is adhered to PET sheet la by optically clear flame retardant adhesive layer 4.
- the embodiment shown in figure 3, like the embodiment of figure 2, includes flame retardant optical coating 2 on a top surface thereof.
- figure 3 only illustrates the presence of a flame retardant optical coating 2 on one surface thereof, it is contemplated that all of the embodiments of the invention may optionally include coating 2 on both exposed surfaces of the composite film (i.e. , on the top surface and the bottom surface).
- coating 2 is on both the top and bottom surfaces of the composite.
- any of the PET sheets used in the present invention may optionally include any conventional dye or light absorber such as a UV light absorber to alter the light transmission characteristics of the composite film.
- PET sheet 1 and/or PET sheet la may optionally include a dye and/or UV absorber.
- one or more of the PET sheets used in the present invention may have a metal coating thereon for affecting the light transmission and/or light reflection or antireflection characteristics of the composite film.
- figure 4 illustrates an embodiment of the invention wherein both PET sheets 1 and la have a metal coating 3 and 3a thereon respectively.
- the embodiment of figure 4 also includes flame retardant optical coating 2 on a top surface thereof.
- the flame retardant optical coating 2 may also be included on the bottom surface thereof.
- Figure 6 shows another embodiment of the invention wherein only one of the PET sheets includes a metal layer thereon.
- the embodiment shown in figure 6 includes PET sheet 1 having a coating of metal 3 thereon.
- the PET sheet la is adhered to the metal coated PET sheet 1 by the flame retardant adhesive layer 4.
- flame retardant optical coating 2 is located on a top surface of the composite film although, as noted above, flame retardant optical coating 2 may be located on both surfaces of the composite film.
- any of the PET sheets may include a dye and/or light absorber (e.g. , UV absorber).
- PET layers 1 and/or la may include a dye or UV absorber incorporated therein.
- PET sheet l includes a dye or UV absorber.
- FIG 7 illustrates an embodiment of the invention which includes three PET sheets 1 , la and lb.
- PET sheet la is shown in figure 7 as having metal coating 3 thereon.
- any of the PET sheets used in the composite films of the present invention may include a metal layer coating thereon.
- Flame retardant optically clear adhesive layers 4 and 4a are used in the embodiment shown in figure 7 for joining PET sheet lb to the metal coated PET sheet la and for joining PET sheet la with PET sheet 1.
- one surface of the composite shown in figure 7 is coated with a flame resistant optical coating 2 although, such a coating may be formed on both surfaces of the composite film.
- Figure 7 illustrates the composite film described in example 4 when PET sheets 1 and lb include a dye as a component thereof.
- Example 1 is for purposes of illustration only and are not drawn to scale to show the thicknesses of the various layers in the composite film.
- This example illustrates the preparation of a flame retardant adhesive composition according to this invention.
- Solutions useful for flame retardant adhesive compositions are prepared by mixing a minor amount by weight of brominated flame retardant polyol, e.g. , tetrabromobisphenol A, and a major amount by weight of a polymeric adhesive precursor, e.g. , isocyanate terminated polyester urethane, in an organic solvent.
- a polymeric adhesive precursor e.g. , isocyanate terminated polyester urethane
- organic solvent a mixture of MEK and toluene.
- a preferred reaction mixture composition comprises 2.4% tetrabromobisphenol A obtained from Albermerle Corporation as Saytex RB- 100 flame retardant, 48.0% isocyanate terminated polyester urethane obtained from Rohm an Haas Inc. as Adcote 527, 33.3 % MEK and 16.6% toluene.
- This example illustrates the preparation of a solvent composition useful for making the flame retardant optical coating layer used in the present invention.
- Solutions useful for making the flame retardant coating are prepared by mixing a minor amount by weight of phosphonate substituted vinyl monomer, e.g. , bis(2-chloroethyl) vinyl phosphonate, and a major amount by weight of a brominated acrylated epoxy polymer.
- phosphonate substituted vinyl monomer e.g. , bis(2-chloroethyl) vinyl phosphonate
- a brominated acrylated epoxy polymer e.g.
- Such vinyl phosphonate monomers are polymerizable by free radical mechanisms.
- compositions are prepared by mixing 10 to 20 parts by weight bis(2- chloroethyl) vinyl phosphonate with 40 to 80 parts by weight of brominated acrylated epoxy oligomer in 10 to 20 parts by weight of organic solvent such as toluene, and up to about 5 parts by weight of polymerization initiator (e.g. , peroxide or sulfonic acid).
- a preferred reaction mixture composition comprises 64 % brominated acrylated epoxy oligomer obtained from UCB Chemicals Corp. as IRR 1031 , 16.8 % bis(2-chloroethyl) vinyl phosphonate obtained from Akzo Nobel Chemicals, Inc.
- This example illustrates the preparation of flame retardant, optically clear composite films of this invention which comprise at least one sheet of polyethylene terephthalate with a flame retardant coating which is the reaction product of brominated acrylated epoxy oligomer and bis(2-chloroethyl) vinyl phosphonate.
- This example further illustrates the use of the flame retardant adhesive composition of this invention to adhere at least two layers of PET film in a composite of this invention.
- a 50 micrometer (2 mil) thick PET film coated with 50 nanometers of aluminum is adhered to a 25 micrometer (1 mil) thick dyed PET film with a 1.5 micrometer thick layer of the adhesive prepared according to example 1.
- the exposed side of the dyed PET film is coated with a 15.6 micrometer thick layer of the coating composition prepared according to example 2.
- the composite film is substantially haze free, i.e. , exhibits less than 25 % haze; is transparent to visible light, i.e. , is transparent to greater than 5 % of incident visible light; and meets the above-noted flame retardant standards of the United Kingdom and Germany.
- Example 4
- This example illustrates a flame retardant, optically clear composite film comprising three layers of PET film.
- a first 25 micrometer (1 mil) thick dyed PET film is coated with a 1.5 micrometer thick layer of flame retardant adhesive prepared according to example 1 and laminated to a 50 micrometer (2 mil) thick PET film coated with a 50 nanometer thick layer of aluminum and a 1.5 micrometer thick layer of the flame retardant adhesive and laminated to a 25 micrometer (1 mil) thick dyed PET film coated with 15.6 micrometer thick flame retardant coating prepared according to example 2.
Landscapes
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Organic Chemistry (AREA)
- General Physics & Mathematics (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Laminated Bodies (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US18985100P | 2000-03-15 | 2000-03-15 | |
US189851P | 2000-03-15 | ||
PCT/US2001/005813 WO2001068360A1 (en) | 2000-03-15 | 2001-03-15 | Flame retardant optical films |
Publications (2)
Publication Number | Publication Date |
---|---|
EP1268189A1 EP1268189A1 (de) | 2003-01-02 |
EP1268189A4 true EP1268189A4 (de) | 2003-04-16 |
Family
ID=22699019
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP01916187A Withdrawn EP1268189A4 (de) | 2000-03-15 | 2001-03-15 | Flammbeständige optische filme |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP1268189A4 (de) |
AU (1) | AU2001243244A1 (de) |
WO (1) | WO2001068360A1 (de) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20100330748A1 (en) | 1999-10-25 | 2010-12-30 | Xi Chu | Method of encapsulating an environmentally sensitive device |
US6623861B2 (en) * | 2001-04-16 | 2003-09-23 | Battelle Memorial Institute | Multilayer plastic substrates |
US8617715B2 (en) | 2003-12-06 | 2013-12-31 | Cpfilms Inc. | Fire retardant shades |
ES2304087B1 (es) * | 2006-05-26 | 2009-05-05 | Comersan, S.A. | Tejido ignifugo con efecto barrera al fuego y procedimiento para su obtencion. |
US20090181242A1 (en) | 2008-01-11 | 2009-07-16 | Enniss James P | Exterior window film |
US9184410B2 (en) | 2008-12-22 | 2015-11-10 | Samsung Display Co., Ltd. | Encapsulated white OLEDs having enhanced optical output |
US9337446B2 (en) | 2008-12-22 | 2016-05-10 | Samsung Display Co., Ltd. | Encapsulated RGB OLEDs having enhanced optical output |
US8999509B2 (en) | 2011-04-27 | 2015-04-07 | Cpfilms Inc. | Weather resistant exterior film composite |
CN104972712A (zh) * | 2014-04-11 | 2015-10-14 | 上海永超真空镀铝有限公司 | 一种遮光复合材料的制备方法 |
CN104972716A (zh) * | 2014-04-11 | 2015-10-14 | 上海永超真空镀铝有限公司 | 一种遮光复合材料 |
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EP0119780A2 (de) * | 1983-03-21 | 1984-09-26 | Stauffer Chemical Company | Elektronischer Interferenz-Abschirmschichtstoff |
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EP0417946A2 (de) * | 1989-09-14 | 1991-03-20 | Imperial Chemical Industries Plc | Kunststoffilm |
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WO1996023658A1 (en) * | 1995-02-03 | 1996-08-08 | Minnesota Mining And Manufacturing Company | Flame retardant ultraviolet cured multi-layered film |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3899621A (en) * | 1971-02-08 | 1975-08-12 | Material Distributors Corp | Security film for shatter-proofing windows |
JPS6084350A (ja) * | 1983-10-14 | 1985-05-13 | Matsushita Electric Works Ltd | 樹脂組成物 |
US4657964A (en) * | 1985-07-03 | 1987-04-14 | Ici Americas Inc. | Aqueous-based urethane coating compositions |
US4634637A (en) * | 1985-11-22 | 1987-01-06 | Gila River Products, Inc. | Solar control film |
US4873309A (en) * | 1987-06-08 | 1989-10-10 | Shell Oil Company | Stabilized flame-retardant epoxy resin composition from a brominated epoxy resin and a vinyl monomer diluent |
CA2106262C (en) * | 1992-10-01 | 2003-11-18 | Ralph H. Bland | Tear resistant multilayer films and articles incorporating such films |
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2001
- 2001-03-15 AU AU2001243244A patent/AU2001243244A1/en not_active Abandoned
- 2001-03-15 WO PCT/US2001/005813 patent/WO2001068360A1/en not_active Application Discontinuation
- 2001-03-15 EP EP01916187A patent/EP1268189A4/de not_active Withdrawn
Patent Citations (8)
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Non-Patent Citations (1)
Title |
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Also Published As
Publication number | Publication date |
---|---|
EP1268189A1 (de) | 2003-01-02 |
AU2001243244A1 (en) | 2001-09-24 |
WO2001068360A1 (en) | 2001-09-20 |
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