Classifications

• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
  • B32B17/06—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
  • B32B17/10—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
  • B32B17/10005—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
  • B32B17/1055—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
  • B32B17/06—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
  • B32B17/10—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
  • B32B17/10005—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
  • B32B17/10009—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the number, the constitution or treatment of glass sheets
  • B32B17/10018—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the number, the constitution or treatment of glass sheets comprising only one glass sheet
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
  • B32B17/06—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
  • B32B17/10—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
  • B32B17/10005—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
  • B32B17/10165—Functional features of the laminated safety glass or glazing
  • B32B17/10174—Coatings of a metallic or dielectric material on a constituent layer of glass or polymer
• • G—PHYSICS
  • G02—OPTICS
  • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
  • G02B5/00—Optical elements other than lenses
  • G02B5/20—Filters
  • G02B5/28—Interference filters
  • G02B5/281—Interference filters designed for the infrared light
  • G02B5/282—Interference filters designed for the infrared light reflecting for infrared and transparent for visible light, e.g. heat reflectors, laser protection
• • G—PHYSICS
  • G02—OPTICS
  • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
  • G02B5/00—Optical elements other than lenses
  • G02B5/20—Filters
  • G02B5/28—Interference filters
  • G02B5/285—Interference filters comprising deposited thin solid films
  • G02B5/287—Interference filters comprising deposited thin solid films comprising at least one layer of organic material
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/25—Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
  • Y10T428/256—Heavy metal or aluminum or compound thereof

Definitions

• the invention relates to a solar control film.
• the most common function is to reduce solar heat load thereby improving comfort and reducing cooling load within a building or a vehicle.
• One type of solar control films known in the art comprises very thin layers of reflecting metal such as silver or aluminium deposited on a transparent substrate.
• the solar control film will have a certain visible light transmission (VLT) and a certain visible light reflection (VLR).
• VLT visible light transmission
• VLR visible light reflection
• the reflecting metal layer must be sufficiently thick. However, by increasing the thickness of the metal layer, the visible light transmission will decrease to a level that is not acceptable.
• An alternative type of solar control films includes an infrared light reflecting multilayer film having alternating layers of a first and a second polymer type.
• the reflection band of this type of selective infrared reflecting films is so close to the visual that a slightly red reflection is observed.
• US2006/154049 describes a multilayer film having an infrared reflecting multilayer having alternating layers of a first and a second polymer and an infrared light absorbing nanoparticles layer dispersed in a cured polymeric binder.
• nanoparticles of various inorganic metal compounds can be used to form coatings that reflect or absorb in a particular wavelength band of the infrared.
• a solar control film is provided.
• the solar control film is positioned relative to the sun and comprises
• the infrared absorbing layer is thereby located further from the sun than the infrared reflecting layer. As the energy of the sun first hits the infrared reflecting layer, part of the energy will be reflected. The part of the energy that is transmitted will be absorbed at least partially by the infrared absorbing layer.
• the nanoparticles are chosen to have an internal transmission of the infrared absorbing layer in the near infrared range lower than 30 % and to have an internal transmission of the infrared absorbing layer in the visible range is higher than 80 %.
• the near infrared range is defined as the range from 780 nm to 2500 nm whereas "the visible range” is defined as the range from 380 to 780 nm.
• a first type of an infrared reflecting layer comprises at least one reflecting metal layer.
• Preferred metal layers comprise aluminium, silver, gold, copper, chromium and alloys thereof.
• Preferred silver alloys comprise silver in combination with for example gold, platinum, palladium, copper, aluminium, indium or zinc and/or mixtures thereof.
• a preferred infrared reflecting layer comprises a silver alloy comprising between 1 and 50 wt% gold, as for example between 10 wt% and 20 wt%.
• An alternative infrared reflecting layer comprises a silver layer or a silver alloy layer having a metal layer such as a gold layer on one or one both sides.
• the thickness of the infrared reflecting layer is preferably ranging between 5 and 25 nm as for example between 5 and 15 nm, such as 7, 8 or 9 nm.
• the infrared reflecting layer is preferably deposited by a vacuum deposition technique for example by sputtering or evaporation.
• the metal layer is sandwiched between layers having a high refractive index such as metal oxides.
• the metal oxide layers may comprise any transparent material.
• metal oxide having a high refractive index and an almost zero extinction coefficient are preferred.
• the infrared reflecting layer may for example comprise one, two or three metal layers, each metal layer sandwiched between layers such as metal oxide layers having a high refractive index.
• the metal oxide layers of the layered structure can be deposited by any technique known in the art.
• Preferred techniques comprise physical vapor deposition techniques such as sputter deposition or chemical vapor deposition techniques.
• a preferred metal oxide layer comprises TiO 2 and more particularly TiO 2 that is mainly composed of rutile phase and that is very dense. This type of TiO 2 has a refractive index of 2.41 at 510 nm.
• a TiO 2 layer can be deposited by a reactive sputter deposition process from a Ti-target, a TiO 2 -target or a substoichiometric TiO x -target (with x between 1.75 and 2).
• TiO 2 mainly composed of rutile phase is preferably deposited by DC magnetron sputtering using a TiO x targets (preferably a rotatable TiO x target) with x between 1.5 and 2, for example between 1.5 and 1.7.
• These rotatable targets are produced by plasma spraying of rutile powder in a reducing atmosphere (e.g. Ar/H 2 ) on a stainless steel backing tube.
• the targets have enough electrical conductivity to be used as cathodes in a DC magnetron sputtering process and can withstand extremely high power levels. As a result, it is possible to achieve very high sputter deposition rates, at lower investment cost (both the deposition source itself and the power supply are considerably cheaper).
• metal oxides having a high refractive index are for example BiO 2 (refractive index 2.45 at 550 nm) or PbO (refractive index 2.55 at 550 nm).
• the different metal oxide layers of the reflecting layer may comprise the same material or may comprise a different material.
• the infrared absorbing layer comprises nanoparticles.
• nanoparticles refers to infrared absorbing inorganic nanoparticles.
• nanoparticles Depending on the infrared absorption resonance wavelength (i.e. the wavelength at which the nanoparticles primarily absorb) and the width of the absorbance range (i.e. the wavelength range over which the nanoparticles cause absorption), one can divide nanoparticles in different groups. a first group of nanoparticles absorb infrared energy in a broad band in the wavelength range above 1000 nm.
• Examples comprise indium oxide, tin oxide, antimony oxide, zinc oxide, aluminium zinc oxide, tungsten oxide, indium tin oxide (ITO) nanoparticles, antimony tin oxide (ATO), antimony indium oxide or combinations thereof.
• ITO indium tin oxide
• ATO antimony tin oxide
• a second group of nanoparticles absorb infrared in the near infrared.
• the nanoparticles of the second group absorb infrared in the range 780 - 1000 nm.
• Examples of nanoparticles of the second group comprise hexaboride nanoparticles, tungsten oxide nanoparticles or composite tungsten oxide particles.
• Tungsten oxide is expressed by the formula W y O z , whereby W is tungsten and O is oxygen and whereby 2 ⁇ z/y ⁇ 3.
• Composite tungsten oxide is expressed by the formula M x W y O z , whereby M is selected from the group consisting of H, He, alkali metal, alkali-earth metals, rare-earth metals , Mg, Zr, Cr, Mn, Fe, Ru, Co, Rh, Ir, Ni, Pd, Pt, Cu, Ag, Au, Zn, Cd, Al, Ga, In , Ti, Si, Ge, Sn, Pb, Sb, B,
• hexaboride particles particles of La, Ho, Dy, Tb, Gd, Nd, Pr, Ce, Y, Sm can be considered.
• the most preferred hexaboride particles comprise LaB 6 .
• hexaboride particles in combination with other particles as for example oxide particles can be considered.
• the second group of nanoparticles is preferred.
• nanoparticles of the second group result in a solar control film combining a remarkable absorption in the near infrared and maintaining a high transmission in the visible.
• the transmission (VLT) in the visible range (380 - 780 nm) is higher than 70 % and more preferably higher than 72 % or even higher than 75 %.
• the transmission in the range 800 - 1000 nm of such an infrared absorbing layer is for all wavelengths of this range below 50 %.
• the above mentioned transmission in the visible range and the transmission in the range 800 -1000 nm is the transmission of an infrared absorbing layer as such, i.e. without any other layer such as an infrared reflecting layer or a substrate.
• a similar infrared absorbing layer comprising nanoparticles of the first group has a lower transmission in the fivisble (380 - 780 nm) and a transmission in the range 800 -1000 nm that is higher than 50 %.
• the nanoparticles have preferably a diameter ranging between 1 nm and 500 nm. More preferably, the diameter of the particles ranges between 10 and 100 nm.
• the nanoparticles can have any shape.
• the concentration of the nanoparticles is preferably ranging between 0.01 and 5 g/m 2 . More preferably, the concentration of the nanoparticles is ranging between 0.8 and 3 g/m 2 .
• the nanoparticles can for example be dispersed in a polymeric binder or they can be incorporated in a substrate such as a polymer film.
• the infrared reflecting layer and the infrared absorbing layer are preferably deposited on a substrate, either a flexible or rigid substrate. Any transparent material conventionally used for solar control films can be considered.
• Preferred substrates comprise glass or polymer films. Suitable polymers are polyethylene terephthalate (PET), polyethylene naphthalate (PEN), polyurethane (PU), polycarbonate (PC), polyimide and polyether imide.
• Figure 1 is a schematic representation of a solar control film according to the present invention
• Figure 2, 3, 4 and 5 show different embodiments of a solar control film according to the present invention.
• Figure 1 shows a schematic representation of a solar control film 10 according to the present invention.
• the solar control film 10 comprises an infrared reflecting layer 12 and an infrared absorbing layer 14.
• the infrared absorbing layer 12 is located further from the sun 16 than the infrared reflecting layer 12.
• the infrared reflecting layer 12 and the infrared absorbing layer are laminated to each other by means of an adhesive 15.
• the solar control film 10 is adhered to a glass substrate 18 by means of an adhesive 17.
• the solar control film comprises an additional layer 19 such as a hard coat layer or a scratch resistant layer.
• FIG. 2 shows a detailed embodiment of a solar control film 20 according to the present invention.
• the solar control film 20 comprises an infrared reflecting layer 21 and an infrared absorbing layer 23.
• the infrared reflecting layer 21 comprises a silver or stabilized silver layer deposited on a first PET substrate 22.
• the infrared absorbing layer 23 is applied on a second PET substrate 24.
• the infrared absorbing layer 23 comprises nanoparticles dispersed in a cured polymeric binder.
• the first PET substrate 22 provided with the infrared reflecting layer 21 and the second PET substrate 24 provided with the infrared absorbing layer 23 are laminated to each other by means of a first adhesive 25 to form the solar control film 20.
• the infrared absorbing layer 23 is thereby brought towards the infrared reflecting layer 21.
• the solar control film comprises an additional layer 26 such as a scratch resistant layer or a hardcoat layer.
• the solar control film 20 is applied to a glass substrate 28 by means of a second adhesive 27.
• Figure 3 shows an alternative embodiment of a solar control film 30 according to the present invention.
• the solar control film 30 comprises an infrared reflecting layer 31 and an infrared absorbing layer 33.
• the infrared reflecting layer comprises a silver or stabilized silver layer
• the infrared absorbing layer 33 is applied on a second PET substrate 34.
• the infrared absorbing layer 33 comprises nanoparticles dispersed in a cured polymeric binder.
• the first PET substrate provided with the infrared reflecting layer 31 and the second PET substrate 34 provided with the infrared absorbing layer 33 are laminated to each other by means of a first adhesive 35 to form the solar control film 30.
• the second PET substrate is thereby brought towards the infrared reflecting layer 31.
• the solar control film comprises an additional layer 36 such as a scratch resistant layer or a hardcoat layer.
• the solar control film 30 is applied to a glass substrate 38 by means of a second adhesive 37.
• Figure 4 shows a further embodiment of a solar control film 40.
• the solar control film 40 comprises an infrared reflecting layer 41 and an infrared absorbing layer 43.
• the infrared reflecting layer 41 comprises a silver or stabilized silver layer 31 deposited on a first PET substrate 42.
• the infrared absorbing layer 43 comprises nanoparticles dispersed in a
• the first PET substrate 42 provided with the infrared reflecting layer 41 and the infrared absorbing layer are laminated to each other by means of a first adhesive 45 to form the solar control film 40.
• the solar control film comprises an additional layer 46 such as a scratch resistant layer or a hardcoat layer.
• the solar control film 20 is applied to a glass substrate 48 by means of a second adhesive 47.
• Figure 5 shows still a further embodiment of a solar control film 50.
• the solar control film 50 comprises an infrared reflecting layer 52 and an infrared absorbing layer 53.
• the infrared reflecting layer 52 comprises a multilayer comprising alternating layers of a first polymer and a second polymer.
• the first polymer and the second polymer have different refractive indices so that some light is reflected at the interfaces between adjacent layers.
• the infrared absorbing layer 53 comprises nanoparticles dispersed in a cured polymeric binder.
• the infrared absorbing layer is applied on a
• the infrared reflecting layer 52 and the PET substrate 54 provided with the infrared absorbing layer 53 are laminated to each other by means of a first adhesive 55 to form solar control film 50.
• the solar control film comprises an additional layer 56 such as a scratch resistant layer or a hardcoat layer.
• the solar control film 50 is applied to a glass substrate 58 by means of a second adhesive 57.
• the solar performance of a number of solar control films according to the present invention is evaluated by determining the visual light transmittance (VLT), the total solar energy rejected (TSER) and the solar heat gain coefficient (SHGC).
• VLT visual light transmittance
• TSER total solar energy rejected
• SHGC solar heat gain coefficient
• the visual light transmittance refers to the percentage of the visible spectrum (380 -780 nm) that is transmitted through a window.
• the total solar energy rejected describes the total amount of incident solar energy (350 - 2500 nm) that is blocked, or rejected, from passing through the window.
• SHGC solar heat gain coefficient
• TSER (I-SHGC) * 100 %
• Film 1 comprises a infrared reflecting silver layer deposited on a PET substrate.
• Film 2 comprises a solar control film according to the present invention comprising a silver layer as infrared reflecting layer and an infrared absorbing layer comprising LaB 6 particles.
• the concentration of the nanoparticles is 0.02 g/m 2 .
• the nanoparticles have a diameter range between 20 and 200 nm with a mean diameter below 80 nm.
• the nanoparticles are dispersed in an UV curable acrylic binder.
• the thickness of the acrylic layer comprising the nanoparticles is 2 ⁇ m.
• Film 3 comprises a solar control film according to the present invention comprising a silver layer as infrared reflection layer and an infrared absorbing layer comprising cesium tungsten oxide nanoparticles.
• concentration of the nanoparticles is 0.3 g/m 2 .
• the nanoparticles have a diameter ranging between 10 and 100 nm as for example 60 nm.
• the nanoparticles are dispersed in an UV curable acrylic binder.
• the thickness of the acrylic layer comprising the nanoparticles is 2 ⁇ m.
• Film 4 comprises a solar control film according to the present invention comprising a silver layer as infrared reflection layer and an infrared absorbing layer comprising cesium tungsten oxide nanoparticles.
• the concentration of the nanoparticles is 1.2 g/m 2 .
• the nanoparticles have a diameter ranging between 10 and 100 nm as for example 60 nm.
• the nanoparticles are dispersed in an UV curable acrylic binder.
• the thickness of the acrylic layer comprising the nanoparticles is 5 ⁇ m. The results are summarized in table 1.
• Film 1 comprising an infrared refecting layer shows a high VLT but a low TSER.
• the TSER is considerably increased while the VLT is reduced only slightly.

Landscapes

• Physics & Mathematics (AREA)
• General Physics & Mathematics (AREA)
• Optics & Photonics (AREA)
• Laminated Bodies (AREA)

Priority Applications (6)

Applications Claiming Priority (2)

Publications (1)

Family

ID=37908362

Family Applications (1)

Country Status (9)

Cited By (3)

Families Citing this family (25)

Citations (4)

Family Cites Families (10)

• 2007
  • 2007-12-13 CN CN200780046150.4A patent/CN101558336A/zh active Pending
  • 2007-12-13 DK DK07857544.6T patent/DK2089743T3/en active
  • 2007-12-13 CN CN201310280722.2A patent/CN103383472B/zh not_active Expired - Fee Related
  • 2007-12-13 JP JP2009540776A patent/JP2010513942A/ja active Pending
  • 2007-12-13 US US12/516,737 patent/US20100062242A1/en not_active Abandoned
  • 2007-12-13 PL PL07857544T patent/PL2089743T3/pl unknown
  • 2007-12-13 EP EP07857544.6A patent/EP2089743B1/en not_active Not-in-force
  • 2007-12-13 AU AU2007331505A patent/AU2007331505B2/en not_active Ceased
  • 2007-12-13 WO PCT/EP2007/063897 patent/WO2008071770A1/en not_active Ceased
  • 2007-12-13 ES ES07857544.6T patent/ES2573934T3/es active Active

Patent Citations (4)

Also Published As

Similar Documents

Legal Events