US20050238886A1 - Coating glass - Google Patents
Coating glass Download PDFInfo
- Publication number
- US20050238886A1 US20050238886A1 US11/170,451 US17045105A US2005238886A1 US 20050238886 A1 US20050238886 A1 US 20050238886A1 US 17045105 A US17045105 A US 17045105A US 2005238886 A1 US2005238886 A1 US 2005238886A1
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- US
- United States
- Prior art keywords
- underlayer
- deposited
- coated glass
- glass
- reflective metal
- 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.)
- Abandoned
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- 239000011521 glass Substances 0.000 title claims abstract description 80
- 238000000576 coating method Methods 0.000 title claims description 25
- 239000011248 coating agent Substances 0.000 title claims description 18
- 229910052751 metal Inorganic materials 0.000 claims abstract description 43
- 239000002184 metal Substances 0.000 claims abstract description 43
- 238000000034 method Methods 0.000 claims abstract description 42
- 239000000758 substrate Substances 0.000 claims abstract description 27
- 239000004332 silver Substances 0.000 claims abstract description 24
- 229910052709 silver Inorganic materials 0.000 claims abstract description 24
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims abstract description 23
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 22
- 229910052814 silicon oxide Inorganic materials 0.000 claims abstract description 22
- 238000000151 deposition Methods 0.000 claims abstract description 21
- 238000010438 heat treatment Methods 0.000 claims abstract description 15
- 238000004519 manufacturing process Methods 0.000 claims abstract description 13
- 238000001771 vacuum deposition Methods 0.000 claims abstract description 12
- 230000008021 deposition Effects 0.000 claims abstract description 10
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 claims abstract description 9
- 230000001590 oxidative effect Effects 0.000 claims abstract description 8
- 239000011787 zinc oxide Substances 0.000 claims abstract description 8
- 238000005137 deposition process Methods 0.000 claims abstract description 7
- 229910044991 metal oxide Inorganic materials 0.000 claims abstract description 6
- 150000004706 metal oxides Chemical class 0.000 claims abstract description 6
- 229910001887 tin oxide Inorganic materials 0.000 claims abstract description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 13
- 239000001301 oxygen Substances 0.000 claims description 13
- 229910052760 oxygen Inorganic materials 0.000 claims description 13
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 11
- 230000005540 biological transmission Effects 0.000 claims description 11
- 229910052799 carbon Inorganic materials 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 8
- 239000012530 fluid Substances 0.000 claims description 7
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 6
- 229910052710 silicon Inorganic materials 0.000 claims description 6
- 239000010703 silicon Substances 0.000 claims description 6
- 239000005329 float glass Substances 0.000 claims description 5
- 230000002000 scavenging effect Effects 0.000 claims description 5
- 229910052782 aluminium Inorganic materials 0.000 claims description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 4
- 239000010410 layer Substances 0.000 description 82
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 26
- 239000000463 material Substances 0.000 description 7
- 238000004544 sputter deposition Methods 0.000 description 6
- 238000005229 chemical vapour deposition Methods 0.000 description 5
- 229910001026 inconel Inorganic materials 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 239000008246 gaseous mixture Substances 0.000 description 4
- 239000004411 aluminium Substances 0.000 description 3
- 238000005452 bending Methods 0.000 description 3
- 230000015556 catabolic process Effects 0.000 description 3
- 238000006731 degradation reaction Methods 0.000 description 3
- 239000011241 protective layer Substances 0.000 description 3
- 238000005546 reactive sputtering Methods 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
- 230000004888 barrier function Effects 0.000 description 2
- 239000011247 coating layer Substances 0.000 description 2
- 230000002950 deficient Effects 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 229920006384 Airco Polymers 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- HRPKYGWRFPOASX-UHFFFAOYSA-N [Zn].[Ag].[Sn] Chemical compound [Zn].[Ag].[Sn] HRPKYGWRFPOASX-UHFFFAOYSA-N 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 239000012159 carrier gas Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000005357 flat glass Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 239000005340 laminated glass Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000001755 magnetron sputter deposition Methods 0.000 description 1
- 229910001120 nichrome Inorganic materials 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 238000005240 physical vapour deposition Methods 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000001314 profilometry Methods 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 238000002310 reflectometry Methods 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000009718 spray deposition Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Images
Classifications
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- 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
- C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
- C03C17/34—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
- C03C17/36—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal
- C03C17/3602—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer
- C03C17/3613—Coatings of type glass/inorganic compound/metal/inorganic compound/metal/other
-
- 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
- C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
- C03C17/34—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
- C03C17/36—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal
-
- 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
- C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
- C03C17/34—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
- C03C17/36—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal
- C03C17/3602—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer
- C03C17/3626—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer one layer at least containing a nitride, oxynitride, boronitride or carbonitride
-
- 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
- C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
- C03C17/34—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
- C03C17/36—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal
- C03C17/3602—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer
- C03C17/3634—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer one layer at least containing carbon, a carbide or oxycarbide
-
- 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
- C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
- C03C17/34—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
- C03C17/36—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal
- C03C17/3602—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer
- C03C17/3639—Multilayers containing at least two functional metal layers
-
- 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
- C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
- C03C17/34—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
- C03C17/36—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal
- C03C17/3602—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer
- C03C17/3644—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer the metal being silver
-
- 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
- C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
- C03C17/34—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
- C03C17/36—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal
- C03C17/3602—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer
- C03C17/3649—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer made of metals other than silver
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- 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
- C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
- C03C17/34—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
- C03C17/36—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal
- C03C17/3602—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer
- C03C17/3657—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer the multilayer coating having optical properties
- C03C17/366—Low-emissivity or solar control coatings
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- 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
- C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
- C03C17/34—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
- C03C17/36—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal
- C03C17/3602—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer
- C03C17/3681—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer the multilayer coating being used in glazing, e.g. windows or windscreens
Definitions
- This invention relates to a process for the production of a heat-treatable low emissivity coated glass and to a heat-treatable low emissivity coated glass.
- transparent glass substrates with a thin reflective metal coating may be produced with low emissivity and a high visible light transmission i.e. which reflect a high proportion of infrared radiation incident upon them but allow visible radiation to pass through.
- the use of such coatings on window glass leads to a reduction in heat loss.
- the silver layers are sandwiched between thin anti-reflection layers of metal oxide.
- Such low emissivity coatings are produced by vacuum deposition processes, especially sputtering, and normally comprise a thin layer of silver sandwiched between two layers of metal oxide. Such coatings are described, for example, in UK patent specification GB 2 129 831.
- a process for the production of a heat-treatable low emissivity coated glass that comprises the steps of:
- the underlayer deposited by a pyrolytic deposition process provides protection to the reflective metal layer on heat-treatment despite its position underneath the reflective metal layer.
- a barrier layer is unnecessary which is advantageous because then fewer layers need be deposited reducing the time needed for the process and so increasing production rates.
- Low emissivity coatings as discussed herein are those which have a normal emissivity of below about 0.4. The lower the emissivity of the coated glass the better are the heat rejecting properties of the glass.
- the reflective metal layer is deposited directly on the underlayer, but one or more intermediate layers (e.g. of metal oxide) may be deposited between the underlayer and the reflective metal layer if, for example it is desired to deposit an anti-reflection layer or anti-reflection layers additional to the underlayer. Layers may also be deposited beneath the underlayer.
- intermediate layers e.g. of metal oxide
- Pyrolytic deposition processes are processes which are usually carried out at substantially atmospheric pressure wherein a fluid is directed onto a hot substrate under conditions such that a coating is formed on the substrate.
- Processes wherein the fluid is a liquid are termed spray deposition processes and processes wherein the fluid is a vapour are termed chemical vapour deposition (CVD) processes.
- the preferred pyrolytic deposition process for deposition of the underlayer is CVD because it may be performed on line (i.e. during the float glass production process) and produces good quality coating layers.
- the underlayer may comprise silicon oxide, silicon oxide containing carbon (often referred to as silicon oxycarbide and which may be deposited as described in European Patent Application 275 662 A), silicon oxide containing nitrogen (often referred to as silicon oxynitride and which may be deposited as described in GB patent 2 031 756 B), titanium oxide, tin oxide, titanium nitride, silicon nitride, silicon carbide, silicon or a mixture comprising one or more of these materials.
- the preferred underlayer comprises a silicon oxide, especially a silicon oxide containing carbon, because silicon oxide layers are relatively easily deposited by CVD in a range of stoichiometries (and hence a range of refractive indices).
- pyrolytically depositing the underlayer preferably comprises contacting the glass substrate with a fluid mixture containing a silicon source, an oxygen source and a carbon source under conditions such that a silicon oxide layer, preferably containing carbon, is deposited.
- the fluid mixture is a vapour mixture.
- the underlayer will usually be deposited on the glass substrate when the glass substrate is at a temperature in the range 450° C. to 800° C., especially when the glass substrate is at a temperature in the range 600° C. to 780° C.
- the underlayer is deposited on to a glass ribbon during the float glass production process at substantially atmospheric pressure in which case the glass ribbon will usually be cut into sheets after deposition of the underlayer (and before deposition of other layers including the reflective metal and any subsequent layers) for storage or convenient transport from the float glass production facility to the vacuum deposition facility.
- the reflective metal layer may comprise silver or aluminium, preferably silver.
- a vacuum deposition process is one which is usually performed at a pressure of lower than about 0.1 mbar and includes such methods as sputtering, reactive sputtering, evaporation and other forms of physical vapour deposition.
- the preferred vacuum deposition method for depositing a reflective metal layer is sputtering.
- an anti-reflection layer is deposited by a vacuum deposition process on to the coated glass after deposition of the reflective metal layer.
- the anti-reflection layer comprises a metal oxide, more preferably the anti-reflection layer comprises zinc oxide or tin oxide. More than one anti-reflection layer may be deposited.
- an anti-reflection layer is deposited by reactive sputtering in an oxidizing atmosphere comprising, for example, more than 70% by volume oxygen
- a further protective layer is preferably deposited on the reflective metal layer before the sputtering step so as to protect the reflective metal layer from degradation by the oxidizing atmosphere.
- the further protective layer preferably comprises inconel or nichrome. Other layers may also be deposited between the reflective metal layer and anti-reflection layer(s).
- the invention also provides a process for the production of coated glass having a coating with more than one reflective metal layer.
- a second reflective metal layer and a second anti-reflection layer are sequentially deposited by a vacuum deposition process after deposition of the first anti-reflection layer.
- the glass will usually have lower emissivity than in the single reflective metal layer embodiment and also, with appropriate layer thicknesses, a reduced transmission of solar heat.
- the process may additionally comprise a heat treatment step wherein the heat-treatable low emissivity coated glass is subjected to a temperature in the range 400° C. to 750° C. in an oxidizing atmosphere, which is usually directed to the production of bent and/or toughened coated glass.
- a heat treatment step wherein the heat-treatable low emissivity coated glass is subjected to a temperature in the range 400° C. to 750° C. in an oxidizing atmosphere, which is usually directed to the production of bent and/or toughened coated glass.
- the visible transmission of the heat-treatable low emissivity coated glass may be increased by the heat-treatment step.
- the invention provides a heat-treatable low emissivity coated glass comprising a glass substrate having a multilayer coating on a surface, said multilayer coating comprising a pyrolytically deposited underlayer, a vacuum deposited reflective metal layer and a vacuum deposited anti-reflection layer.
- the underlayer comprises a silicon oxide, more preferable a silicon oxide containing carbon and advantageously, the underlayer will have a refractive index in the range 1.5 to 3 because an underlayer with a refractive index in this range enables a coating with a low visible light reflection to be produced (i.e. this range of refractive index is suitable for an anti-reflection underlayer).
- the underlayer has a thickness in the range 30 to 100 nm.
- the reflective metal layer usually comprises silver or aluminium and preferably has a thickness in the range 5 to 30 nm, more preferably in the range 7 to 18 nm. At thicknesses lower than 7 nm the reflective metal layer may be discontinuous (this results from the growth mechanism of a layer and may occur even on a flat substrate) and will then not possess the properties of the bulk metal (resulting in poor infra red reflecting properties), whereas thicknesses higher than 18 nm may cause the coated glass to have too high a reflectivity to visible light.
- the anti-reflection layer beneficially has a thickness in the range 30 nm to 90 nm.
- Coated glass according to the invention will usually have a normal emissivity of below 0.2, preferably below 0.1.
- Coated glass according to the invention which has been heat treated by heating it to a temperature in the range 400 to 700° C. in an oxidizing atmosphere will usually have a normal emissivity of below 0.2, preferably below 0.1, after the heat treatment step.
- heat treatment tends to reduce the emissivity of those embodiments of the invention having a single reflective metal layer.
- a heat-treatable low emissivity coated glass comprises a glass substrate having a multilayer coating on one surface, said multilayer coating comprising an oxygen scavenging underlayer, a vacuum deposited reflective metal layer and a vacuum deposited anti-reflection layer.
- the oxygen scavenging underlayer may comprise a material deficient in oxygen that has the potential to bind oxygen in preference to the reflective metal layer (usually a silver layer).
- An example of a material likely to be suitable as an oxygen scavenging underlayer is oxygen deficient silicon oxide (SiO x where x is less than 2).
- Coated glasses produced by the process of the present invention have uses in many areas of glass use including as a glazing pane in a multiple glazing unit or as a glazing pane in a laminated glass which will also comprise a polymer interlayer (usually of polyvinylbutyral) and a second glazing pane.
- a polymer interlayer usually of polyvinylbutyral
- FIG. 1 illustrates schematically a section through a coated glass having a single reflective metal layer, the coated glass produced by a process according to the invention.
- FIG. 2 illustrates schematically a section through a coated glass having two reflective metal layers, the coated glass produced by a process according to the invention.
- a low emissivity coated glass 2 with a single silver layer 8 comprises a glass substrate 4 , a pyrolytically deposited underlayer 6 of silicon oxide containing carbon of thickness 58 nm, a DC magnetron vacuum sputtered silver layer 8 of thickness 12 nm and a further layer of sputtered zinc oxide 10 of thickness 38 nm.
- the underlayer 6 is deposited by on line chemical vapour deposition.
- the underlayer 6 and the zinc oxide layer 10 act as anti-reflection layers.
- a low emissivity coated glass 12 with two silver layers 18 and 22 comprises a glass substrate 14 , a pyrolytically deposited underlayer 16 of silicon oxide containing carbon of thickness 58 nm, and DC magnetron vacuum sputtered layers of: silver 18 of thickness 8.1 nm, zinc oxide 20 of thickness 85 nm, silver 22 of thickness 8.4 nm, and zinc oxide 24 of thickness 49 nm.
- a two silver layer low emissivity coating can provide greater infrared reflection compared to a single silver layer low emissivity coating and can also provide good solar control properties (i.e. reducing transmitted solar heat).
- the silicon oxycarbide (silicon oxide containing carbon) underlayer was deposited substantially as described in European patent application EP 0 275 662A by applying a flowing gaseous mixture to the upper surface of a glass ribbon during the float glass production process using a water-cooled graphite coater.
- the gaseous mixture was applied at a position where the glass temperature was approximately 773° C. as the ribbon advanced at a ribbon speed of 127 m/hr over the float bath.
- the gaseous mixture comprised nitrogen (as carrier gas, flow rate 0.92 kg/hr), monosilane (SiH 4 , flow rate 0.06 kg/hr), ethylene (flow rate 1.84 kg/hr) and carbon dioxide (flow rate 2.31 kg/hr).
- the gaseous mixture was caused to flow parallel to the glass surface in the direction of movement of the glass under laminar flow conditions using an apparatus as described in GB patent specification 1 507 966 extending over the 2 m width of the glass ribbon, and with a path of travel extending approximately 0.1 m down-ribbon.
- the thickness of the glass was about 2.8 mm.
- Table 3 describes the optical properties of the coated glasses of the examples before and after (the values after heat treatment are in brackets) heat treatment to simulate toughening.
- the heat treatment consisted of subjecting the coated glass to a temperature of 640° C. in air for 1.5 minutes.
- the visible transmission, reflection and the transmission and reflection colors in Table 3 were measured using an Hitachi U400 spectrophotometer and/or a Perkin Elmer 883 spectrophotometer, and calculated using the methods described in International Standard ISO 12092:1994(F) and other standard methods.
- the thicknesses of the layers were determined by computer fitting the spectra and by profilometry (Sloan Dektak II profilometer) after appropriate etching treatment (e.g. with aqueous hydrofluoric acid).
- Example 1 Example 2
- Example 3 Silicon Oxide 58 58 58 58 Underlayer (nm) First Silver Layer (nm) 11.9 8.1 11.4 7.9 First Inconel Layer (nm) — — 0.65 0.56 First Dielectric Layer 38 85 43 83 (nm) (Zn0) (Zn0) (Sn0 2 ) (Sn0 2 ) Second Silver Layer — 8.4 — 8.8 (nm) Second Inconel Layer — — 0.54 (nm) Second Dielectric — 49 — 48 Layer (nm) (Zn0) (Sn0 2 )
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Abstract
A process for the production of a heat-treatable low emissivity coated glass that comprises the steps of depositing an underlayer onto a glass substrate and subsequently depositing a reflective metal layer by a vacuum deposition process, wherein the underlayer is deposited by a pyrolytic deposition process. Preferably an anti-reflection layer is deposited by a vacuum deposition process on to the coated glass after deposition of the reflective metal layer. The underlayer may comprise a silicon oxide, the reflective metal layer may comprise silver and the anti-reflection layer may comprise a metal oxide, especially tin oxide or zinc oxide. The coated glass preferably has an emissivity of below 0.2 after heat treatment in an oxidizing atmosphere.
Description
- This application is a continuation application of U.S. application Ser. No. 09/856,584, filed May 23, 2001, which was a 371 application of PCT application Ser. No. PCT/GB99/03984, filed Nov. 30, 1999. U.S. application Ser. No. 09/856,584 was pending as of the filing date of the present application. U.S. application Ser. No. 09/856,584 is hereby incorporated by reference as if set forth in its entirety herein.
- This invention relates to a process for the production of a heat-treatable low emissivity coated glass and to a heat-treatable low emissivity coated glass.
- It is known that transparent glass substrates with a thin reflective metal coating, typically silver 5 nm to 30 nm thick, may be produced with low emissivity and a high visible light transmission i.e. which reflect a high proportion of infrared radiation incident upon them but allow visible radiation to pass through. The use of such coatings on window glass leads to a reduction in heat loss. For optimum light transmission, the silver layers are sandwiched between thin anti-reflection layers of metal oxide. Such low emissivity coatings are produced by vacuum deposition processes, especially sputtering, and normally comprise a thin layer of silver sandwiched between two layers of metal oxide. Such coatings are described, for example, in UK
patent specification GB 2 129 831. - Unfortunately, such low emissivity coatings are not stable to heating in air, and the coating loses its properties of low emissivity and high light transmission when the coated glass is subjected to a thermal cycle which cycle is required for bending or toughening the glass. To obtain a toughened or bent glass substrate bearing a low emissivity reflective metal coating that has high light transmission it has been necessary to either bend and/or toughen the glass before depositing the reflective metal coating or to deposit an additional, protective layer over the reflective metal layer before bending/toughening. GB
patent 2 186 001B describes this problem and a process for the production of a bent and/or toughened silver coated glass substrate wherein an additional metal layer of aluminium, titanium, zinc or tantalum is deposited over the silver layer. The additional metal layer protects the silver layer beneath it from degradation during the bending or toughening thermal cycle by acting as a barrier layer between the silver layer and the oxidizing atmosphere. - The applicants have now discovered that the above problem may be alleviated by depositing an underlayer onto glass substrate using a pyrolytic deposition process and subsequently depositing a reflective metal layer onto the coated substrate.
- According to one aspect of the present invention there is provided a process for the production of a heat-treatable low emissivity coated glass that comprises the steps of:
-
- a) depositing an underlayer onto a glass substrate; and
- b) subsequently depositing a reflective metal layer by a vacuum deposition method, characterized in that the underlayer is deposited by a pyrolytic deposition process.
- Surprisingly, the underlayer deposited by a pyrolytic deposition process provides protection to the reflective metal layer on heat-treatment despite its position underneath the reflective metal layer. In preferred embodiments of the invention a barrier layer is unnecessary which is advantageous because then fewer layers need be deposited reducing the time needed for the process and so increasing production rates.
- Normal emissivity is defined in International Standard ISO 12092:1994(F), Annex A as εN=1−RN where RN is the normal reflectance over the wavelength range 5.5 μm to 50 μm at 283 K. Low emissivity coatings as discussed herein are those which have a normal emissivity of below about 0.4. The lower the emissivity of the coated glass the better are the heat rejecting properties of the glass.
- Usually, the reflective metal layer is deposited directly on the underlayer, but one or more intermediate layers (e.g. of metal oxide) may be deposited between the underlayer and the reflective metal layer if, for example it is desired to deposit an anti-reflection layer or anti-reflection layers additional to the underlayer. Layers may also be deposited beneath the underlayer.
- Pyrolytic deposition processes are processes which are usually carried out at substantially atmospheric pressure wherein a fluid is directed onto a hot substrate under conditions such that a coating is formed on the substrate. Processes wherein the fluid is a liquid are termed spray deposition processes and processes wherein the fluid is a vapour are termed chemical vapour deposition (CVD) processes. The preferred pyrolytic deposition process for deposition of the underlayer is CVD because it may be performed on line (i.e. during the float glass production process) and produces good quality coating layers.
- It is thought that any pyrolytically deposited material could be advantageously used as an underlayer in the present invention. For example, the underlayer may comprise silicon oxide, silicon oxide containing carbon (often referred to as silicon oxycarbide and which may be deposited as described in European Patent Application 275 662 A), silicon oxide containing nitrogen (often referred to as silicon oxynitride and which may be deposited as described in
GB patent 2 031 756 B), titanium oxide, tin oxide, titanium nitride, silicon nitride, silicon carbide, silicon or a mixture comprising one or more of these materials. The preferred underlayer comprises a silicon oxide, especially a silicon oxide containing carbon, because silicon oxide layers are relatively easily deposited by CVD in a range of stoichiometries (and hence a range of refractive indices). - If silicon oxide is selected as the underlayer material, pyrolytically depositing the underlayer preferably comprises contacting the glass substrate with a fluid mixture containing a silicon source, an oxygen source and a carbon source under conditions such that a silicon oxide layer, preferably containing carbon, is deposited. Preferably, the fluid mixture is a vapour mixture.
- The underlayer will usually be deposited on the glass substrate when the glass substrate is at a temperature in the range 450° C. to 800° C., especially when the glass substrate is at a temperature in the range 600° C. to 780° C.
- Preferably, the underlayer is deposited on to a glass ribbon during the float glass production process at substantially atmospheric pressure in which case the glass ribbon will usually be cut into sheets after deposition of the underlayer (and before deposition of other layers including the reflective metal and any subsequent layers) for storage or convenient transport from the float glass production facility to the vacuum deposition facility.
- The reflective metal layer may comprise silver or aluminium, preferably silver.
- A vacuum deposition process is one which is usually performed at a pressure of lower than about 0.1 mbar and includes such methods as sputtering, reactive sputtering, evaporation and other forms of physical vapour deposition. The preferred vacuum deposition method for depositing a reflective metal layer is sputtering.
- Usually, an anti-reflection layer is deposited by a vacuum deposition process on to the coated glass after deposition of the reflective metal layer. Preferably, the anti-reflection layer comprises a metal oxide, more preferably the anti-reflection layer comprises zinc oxide or tin oxide. More than one anti-reflection layer may be deposited.
- If an anti-reflection layer is deposited by reactive sputtering in an oxidizing atmosphere comprising, for example, more than 70% by volume oxygen, a further protective layer is preferably deposited on the reflective metal layer before the sputtering step so as to protect the reflective metal layer from degradation by the oxidizing atmosphere. The further protective layer preferably comprises inconel or nichrome. Other layers may also be deposited between the reflective metal layer and anti-reflection layer(s).
- The invention also provides a process for the production of coated glass having a coating with more than one reflective metal layer. Thus, in an embodiment of the invention a second reflective metal layer and a second anti-reflection layer are sequentially deposited by a vacuum deposition process after deposition of the first anti-reflection layer. In this embodiment of the invention (where the coated glass has two reflective metal layers) the glass will usually have lower emissivity than in the single reflective metal layer embodiment and also, with appropriate layer thicknesses, a reduced transmission of solar heat.
- The process may additionally comprise a heat treatment step wherein the heat-treatable low emissivity coated glass is subjected to a temperature in the range 400° C. to 750° C. in an oxidizing atmosphere, which is usually directed to the production of bent and/or toughened coated glass. Surprisingly and advantageously, the visible transmission of the heat-treatable low emissivity coated glass may be increased by the heat-treatment step.
- In a further aspect, the invention provides a heat-treatable low emissivity coated glass comprising a glass substrate having a multilayer coating on a surface, said multilayer coating comprising a pyrolytically deposited underlayer, a vacuum deposited reflective metal layer and a vacuum deposited anti-reflection layer.
- Preferably the underlayer comprises a silicon oxide, more preferable a silicon oxide containing carbon and advantageously, the underlayer will have a refractive index in the range 1.5 to 3 because an underlayer with a refractive index in this range enables a coating with a low visible light reflection to be produced (i.e. this range of refractive index is suitable for an anti-reflection underlayer). In most embodiments of the invention the underlayer has a thickness in the range 30 to 100 nm.
- The reflective metal layer usually comprises silver or aluminium and preferably has a thickness in the range 5 to 30 nm, more preferably in the range 7 to 18 nm. At thicknesses lower than 7 nm the reflective metal layer may be discontinuous (this results from the growth mechanism of a layer and may occur even on a flat substrate) and will then not possess the properties of the bulk metal (resulting in poor infra red reflecting properties), whereas thicknesses higher than 18 nm may cause the coated glass to have too high a reflectivity to visible light.
- The anti-reflection layer beneficially has a thickness in the range 30 nm to 90 nm.
- Coated glass according to the invention will usually have a normal emissivity of below 0.2, preferably below 0.1. Coated glass according to the invention which has been heat treated by heating it to a temperature in the range 400 to 700° C. in an oxidizing atmosphere will usually have a normal emissivity of below 0.2, preferably below 0.1, after the heat treatment step. Surprisingly and advantageously, heat treatment tends to reduce the emissivity of those embodiments of the invention having a single reflective metal layer.
- It is thought that a pyrolytically deposited underlayer reduces oxygen induced degradation during heat treatment in an oxidizing atmosphere by scavenging oxygen that would otherwise attack the silver layer. Underlayers that scavenge oxygen deposited using methods other than pyrolysis may also be useful as underlayers in the inventions.
- Thus, in a further aspect of the present invention a heat-treatable low emissivity coated glass comprises a glass substrate having a multilayer coating on one surface, said multilayer coating comprising an oxygen scavenging underlayer, a vacuum deposited reflective metal layer and a vacuum deposited anti-reflection layer.
- The oxygen scavenging underlayer may comprise a material deficient in oxygen that has the potential to bind oxygen in preference to the reflective metal layer (usually a silver layer). An example of a material likely to be suitable as an oxygen scavenging underlayer is oxygen deficient silicon oxide (SiOx where x is less than 2).
- Coated glasses produced by the process of the present invention have uses in many areas of glass use including as a glazing pane in a multiple glazing unit or as a glazing pane in a laminated glass which will also comprise a polymer interlayer (usually of polyvinylbutyral) and a second glazing pane.
- So that the invention may be better understood reference will now be made to the following drawings in which:
-
FIG. 1 illustrates schematically a section through a coated glass having a single reflective metal layer, the coated glass produced by a process according to the invention. -
FIG. 2 illustrates schematically a section through a coated glass having two reflective metal layers, the coated glass produced by a process according to the invention. - Referring to
FIG. 1 , a low emissivity coatedglass 2 with asingle silver layer 8 comprises aglass substrate 4, a pyrolytically deposited underlayer 6 of silicon oxide containing carbon of thickness 58 nm, a DC magnetron vacuum sputteredsilver layer 8 ofthickness 12 nm and a further layer of sputteredzinc oxide 10 of thickness 38 nm. The underlayer 6 is deposited by on line chemical vapour deposition. The underlayer 6 and thezinc oxide layer 10 act as anti-reflection layers. - Referring to
FIG. 2 , a low emissivity coatedglass 12 with twosilver layers 18 and 22 comprises aglass substrate 14, a pyrolytically depositedunderlayer 16 of silicon oxide containing carbon of thickness 58 nm, and DC magnetron vacuum sputtered layers of: silver 18 of thickness 8.1 nm,zinc oxide 20 of thickness 85 nm,silver 22 of thickness 8.4 nm, andzinc oxide 24 of thickness 49 nm. A two silver layer low emissivity coating can provide greater infrared reflection compared to a single silver layer low emissivity coating and can also provide good solar control properties (i.e. reducing transmitted solar heat). - The invention is further illustrated by the following examples, in which vacuum deposited coatings were applied to glass substrates coated with an underlayer of silicon oxide containing carbon.
- The silicon oxycarbide (silicon oxide containing carbon) underlayer was deposited substantially as described in European patent application EP 0 275 662A by applying a flowing gaseous mixture to the upper surface of a glass ribbon during the float glass production process using a water-cooled graphite coater. The gaseous mixture was applied at a position where the glass temperature was approximately 773° C. as the ribbon advanced at a ribbon speed of 127 m/hr over the float bath. The gaseous mixture comprised nitrogen (as carrier gas, flow rate 0.92 kg/hr), monosilane (SiH4, flow rate 0.06 kg/hr), ethylene (flow rate 1.84 kg/hr) and carbon dioxide (flow rate 2.31 kg/hr). The gaseous mixture was caused to flow parallel to the glass surface in the direction of movement of the glass under laminar flow conditions using an apparatus as described in GB patent specification 1 507 966 extending over the 2 m width of the glass ribbon, and with a path of travel extending approximately 0.1 m down-ribbon. The thickness of the glass was about 2.8 mm.
- At the end of the float line, samples of the glass coated with the underlayer were cut from the glass ribbon. Coating layers were vacuum deposited on the samples at room temperature by sputtering or reactive sputtering using an Airco Temescal ILS 1600 sputtering plant and DC magnetron sputtering using metal targets of 99.9% purity or better. Deposition conditions for layers comprising silver, inconel, tin (IV) oxide and zinc oxide are described in Table 1.
- The layer materials and layer thicknesses for the underlayer and the vacuum deposited coatings in the examples are described in Table 2.
- Table 3 describes the optical properties of the coated glasses of the examples before and after (the values after heat treatment are in brackets) heat treatment to simulate toughening. The heat treatment consisted of subjecting the coated glass to a temperature of 640° C. in air for 1.5 minutes. The visible transmission, reflection and the transmission and reflection colors in Table 3 were measured using an Hitachi U400 spectrophotometer and/or a Perkin Elmer 883 spectrophotometer, and calculated using the methods described in International Standard ISO 12092:1994(F) and other standard methods. The thicknesses of the layers were determined by computer fitting the spectra and by profilometry (Sloan Dektak II profilometer) after appropriate etching treatment (e.g. with aqueous hydrofluoric acid).
TABLE 1 Layer Material Tin Zinc Silver Inconel Oxide Oxide Power Density 0.61 0.36 3.6 3.8 (W/cm2) Gas Pressure 9.3 11.8 6.7 6.8 (10−3 mbar) Gas Composition (%) Ar 100 100 0 30 O2 0 0 100 70 Target - Substrate 11 11 11 11 Distance (cm) Substrate Speed (cm/s) 2.7 2.9 3.1 3.1 Number of passes to 8 8 10 10 obtain: Thickness (A) 102 10 362 340 -
TABLE 2 Layers Example 1 Example 2 Example 3 Example 4 Silicon Oxide 58 58 58 58 Underlayer (nm) First Silver Layer (nm) 11.9 8.1 11.4 7.9 First Inconel Layer (nm) — — 0.65 0.56 First Dielectric Layer 38 85 43 83 (nm) (Zn0) (Zn0) (Sn02) (Sn02) Second Silver Layer — 8.4 — 8.8 (nm) Second Inconel Layer — — — 0.54 (nm) Second Dielectric — 49 — 48 Layer (nm) (Zn0) (Sn02) -
TABLE 3 Example 1 Example 2 Example 3 Example 4 Value before Value before Value before Value before (after) heat (after) heat (after) heat heat treatment treatment treatment treatment Visible Transmission % 76.3 (78.2) 74.1 (74.9) 74.5 (78.1) 3.2 Visible Reflection % 9.5 (9.1) 5.4 (5.2) 10.7 (9.2) 6.4 Transmission Color a* −4.2 (−3.9) −3.9 (−4.2) −5.1 (−3.4) −4.6 b* 5.3 (4.9) 5.1 (5.4) 7.2 (7.4) 6.7 L 91 (92) 88 (88) 89 (91) 86.2 Reflection Color a* 8.2 (7.9) 3.1 (3.5) 10.4 (8.9) 3.4 b* −3.2 (−3.8) 2.5 (3.2) −5.3 (−4.8) 5.5 L 35.2 (33.5) 31.2 (29.5) 38.7 (34.5) 30.2 Normal Emissivity 0.072 (0.069) 0.060 (0.065) 0.076 (0.072) 0.066
Claims (20)
1. A process for the production of a heat-treatable low emissivity coated glass that comprises the steps of:
a) depositing an underlayer onto a glass substrate by a pyrolytic deposition process; and
b) subsequently depositing a reflective metal layer by a vacuum deposition method, directly on the underlayer, wherein the underlayer comprises a silicon oxide.
2. A process according to claim 1 wherein the pyrolytic deposition of the underlayer comprises contacting the glass substrate with a fluid mixture containing a silicon source, an oxygen source and a carbon source under conditions such that a silicon oxide layer is deposited.
3. A process according to claim 2 wherein the fluid mixture is a vapor mixture.
4. A process according to claim 1 wherein the underlayer is deposited on the glass substrate when the glass substrate is at a temperature in the range 450° C. to 800° C.
5. A process according to claim 1 wherein the underlayer is deposited on to a glass ribbon during the float glass production process at substantially atmospheric pressure.
6. A process according to claim 1 wherein the reflective metal layer comprises silver or aluminum.
7. A process according to claim 1 wherein an anti-reflection layer is deposited by a vacuum deposition process on to the coated glass after deposition of the reflective metal layer.
8. A process according to claim 7 wherein the anti-reflection layer comprises a metal oxide.
9. A process according to claim 8 wherein the anti-reflection layer comprises zinc oxide or tin oxide.
10. A process according to claim 7 wherein a second reflective metal layer and a second anti-reflection layer are sequentially deposited by a vacuum deposition process after deposition of the first anti-reflection layer.
11. A process according to claim 1 additionally comprising a heat treatment step wherein the heat-treatable low emissivity coated glass is subjected to a temperature in the range 400 to 750° C. in an oxidizing atmosphere.
12. A process according to claim 11 wherein the visible transmission of the coated glass is increased by the heat-treatment step.
13. A coated glass produced by a process according to claim 1 .
14. A heat-treatable low emissivity coated glass comprising a glass substrate having a multilayer coating on one surface, said multilayer coating comprising a pyrolytically deposited underlayer which comprises a silicon oxide and is deposited directly on the glass, a vacuum deposited reflective metal layer that is deposited directly on the underlayer, and a vacuum deposited anti-reflection layer.
15. A coated glass according to claim 14 wherein the underlayer has a refractive index in the range 1.5 to 3 and a thickness in the range 30 to 100 nm.
16. A coated glass according to claim 14 wherein the reflective metal layer has a thickness in the range 5 to 30 nm.
17. A coated glass according to claim 14 wherein the anti-reflection layer has a thickness in the range 30 nm to 90 nm.
18. A coated glass according to claim 14 wherein the coated glass has a normal emissivity of below 0.2.
19. A heat-treatable low emissivity coated glass comprising a glass substrate having a multilayer coating on one surface, said multilayer coating comprising an oxygen scavenging underlayer comprising a silicon oxide, a vacuum deposited reflective metal layer that is deposited directly on the underlayer, and a vacuum deposited anti-reflection layer.
20. A multiple glazing unit comprising a first glazing pane of a coated glass according to claim 19 and a second glazing pane.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/170,451 US20050238886A1 (en) | 1998-12-01 | 2005-06-29 | Coating glass |
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB9826293.4A GB9826293D0 (en) | 1998-12-01 | 1998-12-01 | Inprovements in coating glass |
| GB9826293.4 | 1998-12-01 | ||
| PCT/GB1999/003984 WO2000032530A1 (en) | 1998-12-01 | 1999-11-30 | Improvements in coating glass |
| US09/856,584 US6955833B1 (en) | 1998-12-01 | 1999-11-30 | Coating glass |
| US11/170,451 US20050238886A1 (en) | 1998-12-01 | 2005-06-29 | Coating glass |
Related Parent Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/GB1999/003984 Continuation WO2000032530A1 (en) | 1998-12-01 | 1999-11-30 | Improvements in coating glass |
| US09/856,584 Continuation US6955833B1 (en) | 1998-12-01 | 1999-11-30 | Coating glass |
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| Publication Number | Publication Date |
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| US20050238886A1 true US20050238886A1 (en) | 2005-10-27 |
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| US09/856,584 Expired - Fee Related US6955833B1 (en) | 1998-12-01 | 1999-11-30 | Coating glass |
| US11/170,451 Abandoned US20050238886A1 (en) | 1998-12-01 | 2005-06-29 | Coating glass |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US09/856,584 Expired - Fee Related US6955833B1 (en) | 1998-12-01 | 1999-11-30 | Coating glass |
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| Country | Link |
|---|---|
| US (2) | US6955833B1 (en) |
| EP (1) | EP1140723B1 (en) |
| AT (1) | ATE232841T1 (en) |
| AU (1) | AU1397200A (en) |
| DE (1) | DE69905496T2 (en) |
| ES (1) | ES2192891T3 (en) |
| GB (1) | GB9826293D0 (en) |
| WO (1) | WO2000032530A1 (en) |
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-
1999
- 1999-11-30 AT AT99973009T patent/ATE232841T1/en not_active IP Right Cessation
- 1999-11-30 ES ES99973009T patent/ES2192891T3/en not_active Expired - Lifetime
- 1999-11-30 WO PCT/GB1999/003984 patent/WO2000032530A1/en not_active Ceased
- 1999-11-30 US US09/856,584 patent/US6955833B1/en not_active Expired - Fee Related
- 1999-11-30 EP EP99973009A patent/EP1140723B1/en not_active Revoked
- 1999-11-30 DE DE69905496T patent/DE69905496T2/en not_active Revoked
- 1999-11-30 AU AU13972/00A patent/AU1397200A/en not_active Abandoned
-
2005
- 2005-06-29 US US11/170,451 patent/US20050238886A1/en not_active Abandoned
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| US4413877A (en) * | 1980-03-10 | 1983-11-08 | Teijin Limited | Selectively light-transmitting laminated structure |
| US5090984A (en) * | 1988-02-26 | 1992-02-25 | Leybold Aktiengesellschaft | Method for producing glass of high transmission in the visible spectral range and low solar energy transmission |
| US5532062A (en) * | 1990-07-05 | 1996-07-02 | Asahi Glass Company Ltd. | Low emissivity film |
| US5505989A (en) * | 1992-07-11 | 1996-04-09 | Pilkington Glass Limited | Method for coating a hot glass ribbon |
| US5935702A (en) * | 1994-12-23 | 1999-08-10 | Saint-Gobain Vitrage | Glass substrates coated with a stack of thin layers having reflective properties in the infra-red and/or solar ranges |
| US5965246A (en) * | 1995-06-01 | 1999-10-12 | Saint-Gobain Vitrage | Transparent substrates coated with a stack of thin layers having reflection properties in the infrared and/or in the solar radiation range |
Cited By (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9322575B2 (en) * | 2007-12-21 | 2016-04-26 | Agc Glass Europe | Solar energy reflector |
| US20110017202A1 (en) * | 2007-12-21 | 2011-01-27 | Agc Glass Europe | Solar energy reflector |
| US9752799B2 (en) * | 2007-12-21 | 2017-09-05 | Agc Glass Europe | Solar energy reflector |
| US10060180B2 (en) | 2010-01-16 | 2018-08-28 | Cardinal Cg Company | Flash-treated indium tin oxide coatings, production methods, and insulating glass unit transparent conductive coating technology |
| US10000411B2 (en) | 2010-01-16 | 2018-06-19 | Cardinal Cg Company | Insulating glass unit transparent conductivity and low emissivity coating technology |
| US10000965B2 (en) | 2010-01-16 | 2018-06-19 | Cardinal Cg Company | Insulating glass unit transparent conductive coating technology |
| WO2012013796A3 (en) * | 2010-07-29 | 2012-06-14 | Agc Glass Europe | Glass substrate with interference colouration for a facing panel |
| WO2012013787A3 (en) * | 2010-07-29 | 2012-06-14 | Agc Glass Europe | Glass substrate with interference colouration for a facing panel |
| BE1020182A3 (en) * | 2010-07-29 | 2013-06-04 | Agc Glass Europe | GLAZING SUBSTRATE WITH INTERFERENTIAL COLORING FOR A PANEL. |
| EA024159B1 (en) * | 2010-07-29 | 2016-08-31 | Агк Гласс Юроп | Glass substrate with interference colouration for a facing panel |
| US9310542B2 (en) | 2010-07-29 | 2016-04-12 | Agc Glass Europe | Glass substrate with interference colouration for a facing panel |
| WO2013101338A1 (en) * | 2011-12-27 | 2013-07-04 | Intermolecular, Inc. | Low-e panels with ternary metal oxide dielectric layer and method for forming the same |
| US9045363B2 (en) | 2011-12-27 | 2015-06-02 | Intermolecular, Inc. | Low-E panels with ternary metal oxide dielectric layer and method for forming the same |
| US8633118B2 (en) * | 2012-02-01 | 2014-01-21 | Tokyo Electron Limited | Method of forming thin metal and semi-metal layers by thermal remote oxygen scavenging |
| US20130196515A1 (en) * | 2012-02-01 | 2013-08-01 | Tokyo Electron Limited | Method of forming thin metal and semi-metal layers by thermal remote oxygen scavenging |
| US8865538B2 (en) | 2012-03-30 | 2014-10-21 | Tokyo Electron Limited | Method of integrating buried threshold voltage adjustment layers for CMOS processing |
| US8865581B2 (en) | 2012-10-19 | 2014-10-21 | Tokyo Electron Limited | Hybrid gate last integration scheme for multi-layer high-k gate stacks |
| US11028012B2 (en) | 2018-10-31 | 2021-06-08 | Cardinal Cg Company | Low solar heat gain coatings, laminated glass assemblies, and methods of producing same |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2000032530A1 (en) | 2000-06-08 |
| DE69905496D1 (en) | 2003-03-27 |
| GB9826293D0 (en) | 1999-01-20 |
| AU1397200A (en) | 2000-06-19 |
| ATE232841T1 (en) | 2003-03-15 |
| DE69905496T2 (en) | 2003-11-20 |
| EP1140723A1 (en) | 2001-10-10 |
| EP1140723B1 (en) | 2003-02-19 |
| US6955833B1 (en) | 2005-10-18 |
| ES2192891T3 (en) | 2003-10-16 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO PAY ISSUE FEE |