The present application discloses thermochromic windows containing a film with multiple layers of alternating refractive index.
Variable transmission windows are of interest for minimizing heat load in buildings when there is direct sunlight and for maximizing daylighting throughout the day even with widely varying sunlight conditions. There is a desire for variable transmission windows to tint with a neutral color. This may require more than one chromogenic layer to achieve the required spectral coverage. Multiple layers are often needed with sunlight responsive thermochromic layers for windows and the use of multiple thermochromic layers to achieve neutral appearance of transmitted light is described in detail in U.S. Pat. No. 7,525,717, the contents of which are hereby incorporated by reference. Whether to achieve neutral coloration or if multiple layers are desired for other reasons, the thermochromic layers used in windows generally must be separated from each other in order to keep the different materials in each layer from diffusing into the other layers. If the materials intermix they could change the performance and possibly the durability of each layer. The separator layer is generally a glass or plastic layer that is impermeable to the materials in the thermochromic layers.
Preferred plastic separator layers for use in thermochromic windows are made of polyolefins like various types of polyethylene and polypropylene, cellulosics like cellulose acetate butyrate and cellulose triacetate, polyester terephthalates like polyethylene terephthalate, acrylics or polycarbonates. Plastic separator layers are typically in the form of films or sheets that are 25 microns to 500 microns thick. Particularly useful glass separators are made of soda lime or borosilicate glass with a thickness of 50 to 6000 microns.
Particularly useful thermochromic materials for use in the thermochromic layers of the present application are termed ligand exchange thermochromic, LETC, materials. LETC materials have thermochromic activity which results in a reversible change in absorbance of electromagnetic radiation as the temperature of the system is reversibly changed. That the change is reversible means that the absorbance increase as the temperature increases is the same as the absorbance decrease as the temperature decreases for a cycle of temperature increase and decrease over a given temperature range. LETC materials of interest for use in practical thermochromic systems, layers and devices are stable on repeated temperature cycling for some useful number of cycles. Particularly useful LETC materials and systems have a net increase in their ability to absorb visible and/or NIR light energy as the temperature of the system increases and a net decrease in their ability to absorb visible and/or NIR light energy as the temperature of the system decreases for temperatures within the active range of the system. The active temperature range of the system is determined by the thermodynamic properties of the LETC reactions. For many particularly useful applications, like sunlight responsive thermochromic windows, the active temperature range includes −20° C. to 100° C.
It is preferred that the electromagnetic radiation, for which absorbance changes occur, be in the ultraviolet or especially the visible and/or NIR portions of the electromagnetic spectrum. The change in light absorption on heating of the LETC systems generally results in a change from one color to another color and/or a darkening of the color of the system. If the increase in light absorption is predominantly in the NIR, the LETC system may still be very useful even though little or no visual color change occurs. However, for most preferred applications of the LETC systems or layers utilized herein, there is a net increase in the ability of the system to absorb incident visible sunlight power (or energy over time), as the temperature of the system increases from T1 to T2 and an equal net decrease in the ability of the system to absorb incident visible sunlight power (or energy over time), as the temperature of the system decreases from T2 to T1. In most cases, this means that the LETC systems become darker in color as the temperature of the system increases and lighter in color as the temperature of the system decreases. In general, there is no change in the amount of light scattered or reflected by the LETC system itself.
U.S. Pat. Nos. 7,525,717; 7,538,931; 7,542,196 and 8,018,639, which describe LETC materials, systems, layers, devices and windows are hereby incorporated into this disclosure by reference. LETC systems comprise one or more than one transition metal ion, such as Fe(II), Co(II), Ni(II) or Cu(II) ions, which experiences thermally induced changes in the nature of the complexation or coordination around the transition metal ion(s) and thereby the system changes its ability to absorb electromagnetic radiation as the temperature changes. As explained in U.S. Pat. Nos. 7,525,717; 7,538,931; 7,542,196 and 8,018,639, LETC systems employ so-called high epsilon ligands, (HεL's), and low epsilon ligands, (LεL's). Upon increasing the temperature of the thermochromic system, layer or device, one or more of the LεL's will be displaced by one or more HεL's to give a complex that absorbs more visible and/or NIR radiation. Examples of LεL's are diols, triols and certain hydroxy containing polymers like poly(vinyl butyral). Examples of HεL's are chloride, bromide, iodide and molecules that coordinate to transition metal ions through one or more than one nitrogen, oxygen, phosphorus or sulfur atom in the HεL molecule.
For the use of LETC systems in applications like variable transmission, energy saving windows, especially Sunlight Responsive Thermochromic, SRT™, windows, there is a demand for certain colors. While fixed tint windows which are gray, green, blue and bronze are in widespread use, the most desirable color, (or lack thereof), for variable tint windows is gray. This is especially true when the window is or is able to become heavily tinted as the view through a heavily tinted gray window maintains the same color rendition for objects viewed through the window as is maintained with a lightly tinted or nearly colorless window. Also it is highly desirable for the daylighting that comes in through the window to be color neutral so that people and objects illuminated by the incoming light have an acceptable appearance.
The systems disclosed here-in are particularly useful when used in combination with the window structures or constructions disclosed in U.S. Pat. Nos. 6,084,702; 6,446,402 and 7,817,328. The contents of these patents are hereby incorporated into this disclosure by reference.
Most previous separators for separating thermochromic layers from each other were generally transparent to visible and near infrared, (NIR), light thus these separators did not contribute to the solar control of the layers when they were used in a thermochromic window. It has been discovered that films with reflection properties in the NIR can be used as separators for thermochromic films. A particularly useful separator film of this type is made up of multiple polymer layers where alternating layers of two or more polymer materials have different indices of refraction. Herein these films are referred to as multiple layers of alternating refractive index, (MLARI), films. If the thickness of the layers and the indices of refraction are properly chosen, these films can reflect portions of the solar spectrum and thereby enhance the performance of a window that incorporates such a film. The reflections of the MLARI film in the NIR is particularly synergistic with the predominately visible light absorbance changes of many thermochromic systems since the combination covers more of the solar spectrum that causes undesirable heat load on buildings. In the present application, it is preferred that the reflectance of MLARI films reflect light or radiation in the NIR region. However, these films may also reflect portions of the UV and/or visible and may have some absorbance in the UV, visible and/or NIR portions of the spectrum and still be effective in enhancing the performance of windows into which these films are incorporated.
MLARI films reflect light or electromagnetic radiation based on the well known principle of dielectric mirrors. As electromagnetic radiation passes from a medium of one index of refraction to another medium with a different index of refraction an amount of the electromagnetic radiation is reflected based on the magnitude of the difference in the indices of refraction between the two media. If the media are in thin alternating layers the reflections of the electromagnetic radiation can constructively or destructively interfere. This interference is dependent on the wavelengths of electromagnetic radiation, the difference in index of refraction between the media and thicknesses of the layers. The media generally have little or no absorption of the electromagnetic radiation involved. The layers may be made up of metal oxides, polymers or combinations thereof.
The layers making up the MLARI film have different refractive index characteristics so that some light is reflected at interfaces between adjacent layers. The layers are sufficiently thin so that light reflected at a plurality of the interfaces undergoes constructive or destructive interference in order to give the film the desired reflective or transmissive properties. For MLARI films designed to reflect light at ultraviolet, visible, or near-infrared wavelengths, each layer generally has an optical thickness (i.e., a physical thickness multiplied by refractive index) of less than about 1 micrometer. Thicker layers can, however, also be included, such as skin layers at the outer surfaces of the film, or protective boundary layers disposed within the film that separate packets of layers.
In accordance with one embodiment of the invention, the MLARI layer is used to separate two or more thermochromic layers. In accordance with another embodiment, the MLARI layer is used in conjunction with one or more thermochromic layers but not as a separator. In this embodiment, a conventional separator may be used to support or separate the thermochromic layers and the MLARI layer may be suspended in a gas space or carried on a separate glass or plastic substrate or pane within the window as illustrated in
The reflective and transmissive properties of the multilayer film are a function of the refractive indices of the respective layers (i.e., microlayers). In practice, the refractive indices are controlled by judicious materials selection and processing conditions. The multilayer film can be made by co-extrusion of typically tens or hundreds of layers of two alternating polymers A, B, followed by optionally passing the multilayer extrudate through one or more multiplication dies, and then stretching or otherwise orienting the extrudate to form a final film. The resulting film is composed of typically tens or hundreds of individual layers whose thicknesses and refractive indices are tailored to provide one or more reflection bands in desired region(s) of the spectrum, such as in the visible, near infrared, and/or infrared.
The multilayer film can be formed by any useful combination of alternating polymer type layers. In many embodiments, at least one of the alternating polymer layers is birefringent and oriented. In some embodiments, one of the alternating polymer layers is birefringent and oriented and the other alternating polymer layer is isotropic. In one embodiment, the multilayer optical film is formed by alternating layers of a first polymer type including polyethylene terephthalate (PET) or copolymer of polyethylene terephthalate (coPET) and a second polymer type including poly(methyl methacrylate) (PMMA) or a copolymer of poly(methyl methacrylate) (coPMMA). In another embodiment, the multilayer optical film is formed by alternating layers of a first polymer type including polyethylene terephthalate and a second polymer type including a copolymer of poly(methyl methacrylate and ethyl acrylate).
In another embodiment, the multilayer film is formed by alternating layers of a first polymer type including cyclohexanedimethanol modified polyester terephthalate (PETG) or a copolymer of cyclohexanedimethanol modified polyester terephthalate (coPETG) and second polymer type including polyethylene naphthalate (PEN) or a copolymer of polyethylene naphthalate (coPEN). In another embodiment, the multilayer optical film is formed by alternating layers of a first polymer type including polyethylene naphthalate or a copolymer of polyethylene naphthalate and a second polymer type including poly(methyl methacrylate) or a copolymer of poly(methyl methacrylate). Useful combinations of alternating polymer type layers are disclosed in U.S. Pat. No. 6,352,761, which is incorporated by reference herein.
For the present application, alternating layers of the following polymers are particularly useful. MLARI films may be provided by alternating layers of for example:
Many other combinations of these and other polymers may be used. The polymer films may have isotropic indices of refraction or one or both films may be birefringent, (i.e., having anisotropic indices of refraction). The advantages of birefringent polymer layers to reduce the angle dependence of the intensity of the reflection of electromagnetic radiation is described in detail in Science 287, pages 2451-2456, (2000). Layer thicknesses are typically in the 75 to 150 nanometer range. The total number of layers is typically between about 100 and 1000. Thedifference between indices of refraction is typically about 0.05 to 0.2 for the two media or polymers making up the MLARI.
Multiple, thin film polymer layers with alternating refractive index which provide selective reflection properties have been known for a number of years and numerous patents describe this technology. Several of the U.S. patents related to this technology: U.S. Pat. Nos. 3,610,724; 3,759,647; 3,773,882; 3,884,606; 4,162,343; 4,310,584; 4,446,305; 4,540,623; 5,103,337; 5,126,880; 5,269,995; 5,278,694; 5,360,659; 5,389,324; 5,448,404; 5,540,978; 5,552,927; 5,882,774; 5,976,424; 6,045,894; 6,088,163; 6,368,699; 6,459,514; 6,531,230; 6,565,982; 6,788,463; 6,827,886; 6,830,713; 6,924,014; 6,999,233; 7,057,816; 7,138,173; 7,147,903; 7,255,914; 7,297,393 and 7,851,054 are hereby incorporated by reference.
Also, U.S. Pat. No. 7,952,805 and the article “Science 287, 2451-2456, (2000)” give good technical descriptions of MLARI films and are hereby incorporated by reference.
If the reflectance provided by the MLARI film is in the NIR, the film can help reflect sunlight energy to the outside of a building while still allowing in desirable daylighting. This is particularly advantageous when the film is used as a separator to separate thermochromic layers that predominantly change transmission in the visible portion of the solar spectrum.
Preferred MLARI separators are “Sun Control Window Films” which are commercially available from 3M of St. Paul, Minn. Examples of particularly useful separators include “Sun Control Window Films” selected from 3M's Prestige Series, Ceramic Series, Night Vision Series or Traditional Series. Sometime these preferred films are referred to as Ultra Clear Solar Film, (UCSF) from 3M.
Certain aspects of the present application are described in more detail in the following non-limiting examples:
A 3 layer stack of: 1) a first thermochromic layer, 2) a MLARI separator, and 3) a second thermochromic layer was placed between 2 sheets of soda-lime float glass and heated under vacuum in vacuum bag lamination apparatus until a uniform laminate was formed. The first thermochromic, poly(vinyl butyral) based layer was light tan at room temperature and turned progressively darker orange on heating to 85° C. The MLARI separator was a UCSF obtained from 3M. The second thermochromic, poly(vinyl butyral) based layer was light blue-green at room temperature and turned progressively darker blue on heating to 85° C. Together the orange and the blue tinting layers provide a relatively neutral appearance for light transmitted through the combination of layers.
Table 1 below shows the durability testing for the laminate of Example 1.
The laminate of Example 1 was placed in an Atlas Electric Weather-ometer and was exposed to light from a xenon arc lamp at 0.55 W/m2 at 340 nanometer with black panel temperature of 85 C. The spectra of the laminate at 25° C. and at 85° C. were measured before exposure and again at each time after the hours of exposure in the Weather-ometer listed in Table 1. From the spectra the color coordinates a* and b* and the CIE white light transmission for D65 designated as Y were calculated. These results are shown in Table 1. The results show that the MLARI layer is acting as an excellent separator for the thermochromic layers by being largely impermeable to the components of the thermochromic layer. Overall the device with this novel separator is showing excellent durability based on the measured data and visual inspection.
The structures disclosed herein can also be utilized with other mechanisms to improve system stability or durability. For example, the teachings herein can be combined with those in U.S. patent application Ser. No. 13/310,357, filed Dec. 2, 2011 entitled “ANTI-YELLOWING FOR THERMOCHROMIC SYSTEMS” which discloses thermochromic systems containing an anti-yellowing agent in an amount sufficient to minimize or eliminate the yellow color formation that is associated with some thermochromic systems. Thermochromic systems susceptible to yellowing are stabilized by inclusion of the anti-yellowing material in the composition. The contents of the '357 application are hereby incorporated by reference.
While it is particularly useful in the present application to use the MLARI films as a separator for the thermochromic layers, at times it is also desirable to use MLARI films in other structures or configurations of thermochromic windows. Several of these structures are shown in
A particularly advantageous structure is shown in
Hard coat low-e coating may be used on the exterior or exposed surfaces of window substrates like glass. The transmission as a function of wavelength for a typical hard coat low-e coating is also shown in
It has been discovered that it is important for polymeric separators like MLARI films to adhere well to the thermochromic layers so that there is no delamination between the films prior to or during the lamination of the stack of thermochromic and separator films between sheets of glass. If the natural adhesion between the separator and thermochromic layer(s) is insufficient, one or more surfaces of the separator may be treated in some manner to promote adhesion. Separators, including MLARI films, may be treated in by one or more of the following processes. The separator may be coated with one or more metal oxides such as oxides of silicon titanium, zinc, tin and indium and mixtures thereof. The separator surfaces may be pretreated, activated or excited by processes such as exposure to ozone, atmospheric plasma treatment with various gases and gas mixtures or by glow discharge, plasma or corona treatment processes in vacuum, partial vacuum, inert atmosphere, oxygen or air. The separator may be coated with adhesion promoting coating of coupling agents, such as silane coupling agents or primers including organic primers such as amines, imine, urethanes, ureas, polyvinylchloride, polyvinylidene chloride, polyallylamines or water based primers.
The present application discloses a multilayer plastic laminate comprising two or more than two thermochromic layers and one or more than one separator layer wherein at least one of the separator layers is a MLARI film.
Another manifestation of this disclosure relates to a multilayer plastic laminate comprising two or more than two thermochromic layers and one or more than one separator layer wherein at least one of the separator layers is a MLARI film and wherein the multilayer plastic laminate is laminated between rigid substrates of glass or plastic.
In accordance with another aspect, this present application provides a multilayer plastic laminate comprising two or more than two thermochromic layers and one or more than one separator layer wherein at least one of the separator layers is a MLARI film and wherein the multilayer plastic laminate is laminated between rigid substrates of glass or plastic and wherein one or more than one of the substrates has a hard coat low-e coating on an exterior surface.
In yet another manifestation, the present application provides is a multilayer plastic laminate comprising two or more than two thermochromic layers and one or more than one separator layer wherein at least one of the separator layers is a MLARI film and wherein the multilayer plastic laminate is laminated between rigid substrates of glass or plastic and wherein one or more than one of the substrates has a hard coat low-e coating on an exterior surface and the laminate is used as monolithic window installed in a building.
In accordance with another aspect, the present application provides a multilayer plastic laminate comprising two or more than two thermochromic layers and one or more than one separator layer wherein at least one of the separator layers is a MLARI film and wherein the multilayer plastic laminate is laminated between rigid substrates of glass or plastic and wherein one or more than one of the substrates has a hard coat and/or a soft coat low-e coating on an exterior surface and the laminate is used as the interior pane or the exterior pane of a double pane insulated glass unit.
In accordance with yet another aspect, the present application provides a thermochromic laminate comprising at least one thermochromic layer between glass or plastic substrates wherein the laminate further comprises a MLARI film on one of the substrates.
In accordance with another aspect, the present application provides a thermochromic laminate comprising at least one thermochromic layer between glass or plastic substrates wherein the laminate further comprises a MLARI film on one of the substrates wherein the laminate is used as a monolithic window pane or as the interior or the exterior pane of a double pane insulated glass unit.
In accordance with another aspect, the present application provides a thermochromic laminate comprising at least one thermochromic layer between glass or plastic substrates wherein the laminate is the interior or the exterior pane of a double pane insulated glass unit and the insulated glass unit comprises a suspended MLARI film which is effective to divide the gas space into two compartments.
Any of the foregoing aspects of the present application may include one or more than one hard coat and/or soft coat low-e layer on any gas or vacuum exposed surface of any substrate or any gas or vacuum exposed surface of a MLARI film.
The present application also provides a system, series of layers, device or window in which a MLARI film is a separator for thermochromic layers.
In accordance with another aspect, the present application provides a window comprising a thermochromic layer and a film comprised of multiple layers of polymer with alternating refractive index wherein the thermochromic layer has a reversible change in absorbance of electromagnetic radiation such that the absorbance increases as the temperature of the thermochromic layer increases and the absorbance decreases at the temperature of the thermochromic layer decreases.
In accordance with another aspect, the present application provides a window comprising more than one thermochromic layer wherein two of the thermochromic layers are adhered to and separated by a film comprised of multiple layers of polymer with alternating refractive index wherein the thermochromic layers each have a reversible change in absorbance of electromagnetic radiation such that the absorbance increases as the temperature of the thermochromic layer increases and the absorbance decreases at the temperature of the thermochromic layer decreases.
In accordance with another aspect, the present application provides a window that is single pane or monolithic window which comprises:
a) a thermochromic layer;
b) a film comprised of multiple layers of polymer with alternating refractive index;
c) a pair of rigid substrates;
d) a hard coat low-e coating on at least one of the substrates;
wherein the thermochromic layer has a reversible change in absorbance of electromagnetic radiation such that the absorbance increases as the temperature of the thermochromic layer increases and the absorbance decreases at the temperature of the thermochromic layer decreases and wherein a thermochromic layer and a film comprised of multiple layers of polymer with alternating refractive index are laminated between the rigid substrates.
In accordance with another aspect, the present application provides a window with a film comprised of multiple layers of polymer with alternating refractive index which has alternating layers of two of the following polymers: cyclohexanedimethanol, a copolymer of cyclohexanedimethanol, polymethylmethacrylate polycarbonate, polyethylene naphthalate, polyethylene terephthalate, polyethylene and polystyrene.
Having described the invention in detail and by reference to preferred embodiments thereof, it will be apparent that modifications and variations are possible without departing from the scope of the invention as defined by the following claims.
Number | Name | Date | Kind |
---|---|---|---|
2710274 | Kuehl | Jun 1955 | A |
3192101 | Koenig | Jun 1965 | A |
3236651 | Marks et al. | Feb 1966 | A |
3445291 | Stein | May 1969 | A |
3610724 | Frizzell | Oct 1971 | A |
3723349 | Heseltine et al. | Mar 1973 | A |
3759647 | Schrenk et al. | Sep 1973 | A |
3773882 | Schrenk | Nov 1973 | A |
3816335 | Evans | Jun 1974 | A |
3884606 | Schrenk | May 1975 | A |
4044519 | Morin et al. | Aug 1977 | A |
4162343 | Wilcox et al. | Jul 1979 | A |
4310584 | Cooper et al. | Jan 1982 | A |
4446305 | Rogers et al. | May 1984 | A |
4540623 | Im et al. | Sep 1985 | A |
4575259 | Bacci et al. | Mar 1986 | A |
4577619 | Howe, Jr. et al. | Mar 1986 | A |
4970315 | Schmidhalter | Nov 1990 | A |
5094055 | Berdan | Mar 1992 | A |
5103337 | Schrenk et al. | Apr 1992 | A |
5126880 | Wheatley et al. | Jun 1992 | A |
5159057 | Perry | Oct 1992 | A |
5240897 | Braun et al. | Aug 1993 | A |
5244602 | Van Gemert | Sep 1993 | A |
5269995 | Ramanathan et al. | Dec 1993 | A |
5278694 | Wheatley et al. | Jan 1994 | A |
5330686 | Smith et al. | Jul 1994 | A |
5340857 | Van Gemert | Aug 1994 | A |
5360659 | Arends et al. | Nov 1994 | A |
5389324 | Lewis et al. | Feb 1995 | A |
5395567 | Van Gemert et al. | Mar 1995 | A |
5448404 | Schrenk et al. | Sep 1995 | A |
5451344 | Knowles et al. | Sep 1995 | A |
5458814 | Kumar et al. | Oct 1995 | A |
5466398 | Van Gemert et al. | Nov 1995 | A |
5525430 | Chahroudi | Jun 1996 | A |
5540978 | Schrenk | Jul 1996 | A |
5547815 | Vanmaele | Aug 1996 | A |
5552090 | Van Gemert et al. | Sep 1996 | A |
5552927 | Wheatly et al. | Sep 1996 | A |
5565147 | Knowles et al. | Oct 1996 | A |
5578252 | Van Gemert et al. | Nov 1996 | A |
5637262 | Van Gemert et al. | Jun 1997 | A |
5645767 | Van Gemert | Jul 1997 | A |
5650098 | Kumar et al. | Jul 1997 | A |
5651923 | Kumar et al. | Jul 1997 | A |
5658500 | Kumar et al. | Aug 1997 | A |
5658501 | Kumar et al. | Aug 1997 | A |
5674432 | Knowles et al. | Oct 1997 | A |
5744056 | Venkateshwaran et al. | Apr 1998 | A |
5753146 | Van Gemert et al. | May 1998 | A |
5869658 | Lin et al. | Feb 1999 | A |
5882774 | Jonza et al. | Mar 1999 | A |
5976424 | Weber et al. | Nov 1999 | A |
6045894 | Jonza et al. | Apr 2000 | A |
6084702 | Byker et al. | Jul 2000 | A |
6088163 | Gilbert et al. | Jul 2000 | A |
6094290 | Crawford et al. | Jul 2000 | A |
6103459 | Diel | Aug 2000 | A |
6106744 | Van Gemert et al. | Aug 2000 | A |
6153422 | Kashiba | Nov 2000 | A |
6348604 | Nelson et al. | Feb 2002 | B1 |
6352761 | Hebrink et al. | Mar 2002 | B1 |
6362303 | Byker et al. | Mar 2002 | B1 |
6368699 | Gilbert et al. | Apr 2002 | B1 |
6373618 | Agrawal et al. | Apr 2002 | B1 |
6391406 | Zenner et al. | May 2002 | B1 |
6446402 | Byker et al. | Sep 2002 | B1 |
6459514 | Gilbert et al. | Oct 2002 | B2 |
6479293 | Tamura et al. | Nov 2002 | B1 |
6531230 | Weber et al. | Mar 2003 | B1 |
6565982 | Ouderkirk et al. | May 2003 | B1 |
6594067 | Poll et al. | Jul 2003 | B2 |
6620872 | Fisher | Sep 2003 | B2 |
6630597 | Lin et al. | Oct 2003 | B1 |
6665107 | Forgette et al. | Dec 2003 | B2 |
6737159 | Garrett et al. | May 2004 | B2 |
6737418 | Hogenkamp et al. | May 2004 | B2 |
6788463 | Merrill et al. | Sep 2004 | B2 |
6827886 | Neavin et al. | Dec 2004 | B2 |
6830713 | Hebrink et al. | Dec 2004 | B2 |
6924014 | Ouderkirk et al. | Aug 2005 | B2 |
6998072 | Welch et al. | Feb 2006 | B2 |
6999233 | Allen et al. | Feb 2006 | B2 |
7057816 | Allen et al. | Jun 2006 | B1 |
7094368 | Kim et al. | Aug 2006 | B2 |
7138173 | Wheatley et al. | Nov 2006 | B2 |
7147903 | Ouderkirk et al. | Dec 2006 | B2 |
7179535 | Fisher | Feb 2007 | B2 |
7226966 | Kambe et al. | Jun 2007 | B2 |
7255914 | Shirk et al. | Aug 2007 | B2 |
7256296 | Diamond et al. | Aug 2007 | B2 |
7297393 | Jonza et al. | Nov 2007 | B2 |
7320826 | Kumar et al. | Jan 2008 | B2 |
7525717 | Byker et al. | Apr 2009 | B2 |
7538931 | Byker et al. | May 2009 | B2 |
7542196 | Byker et al. | Jun 2009 | B2 |
7556750 | Xiao et al. | Jul 2009 | B2 |
7556751 | Chopra et al. | Jul 2009 | B2 |
7560056 | Van Gemert et al. | Jul 2009 | B2 |
7584630 | Van Gemert | Sep 2009 | B2 |
7727633 | Kirkman et al. | Jun 2010 | B2 |
7817328 | Millett et al. | Oct 2010 | B2 |
7851054 | Weber et al. | Dec 2010 | B2 |
7911676 | Knowles et al. | Mar 2011 | B2 |
7952805 | McGurran et al. | May 2011 | B2 |
7985456 | Stewart et al. | Jul 2011 | B2 |
8003751 | Share et al. | Aug 2011 | B2 |
8018639 | Byker et al. | Sep 2011 | B2 |
8154788 | Millett et al. | Apr 2012 | B2 |
8182718 | Byker et al. | May 2012 | B2 |
8248683 | Lee et al. | Aug 2012 | B2 |
8248693 | Cook | Aug 2012 | B2 |
8431045 | Byker et al. | Apr 2013 | B2 |
8623243 | Anderson et al. | Jan 2014 | B2 |
20060159874 | Koran et al. | Jul 2006 | A1 |
20080092456 | Millett et al. | Apr 2008 | A1 |
20080100902 | Byker et al. | May 2008 | A1 |
20080100903 | Byker et al. | May 2008 | A1 |
20080105851 | Byker et al. | May 2008 | A1 |
20080106781 | Byker et al. | May 2008 | A1 |
20100270519 | Blackman et al. | Oct 2010 | A1 |
20110075244 | Millett et al. | Mar 2011 | A1 |
20120001134 | Byker et al. | Jan 2012 | A1 |
20130286461 | Broekhuis et al. | Oct 2013 | A1 |
20130310357 | Liu | Nov 2013 | A1 |
Number | Date | Country |
---|---|---|
0356116 | Feb 1990 | EP |
H02-180973 | Jul 1990 | JP |
2004-359623 | Dec 2004 | JP |
2008028099 | Mar 2008 | WO |
2008028128 | Mar 2008 | WO |
Entry |
---|
Arutjunjan, R. et al., “Smart Thermochromic Glazing for Energy Saving Window Applications,” Poster Session Abstract 8, The Fourth International Conference on Advanced Optical Materials and Devices, Tartu, Estonia (Jul. 6-9, 2004). |
Kojima, K. et al., “Pressure and Temperature Effects on Octahedral-Tetrahedral Equilibria in Pyridine Solutions of Some Cobalt(II) Halides. II,” Bull. Chem. Soc. Jpn., vol. 57, No. 3, pp. 879-880 (Mar. 1984). |
Yanush, O.V. et al., “Laminated Glass with Variable Transmission for Daylight Regulation,” Glass Processing Days, Conference Proceedings, pp. 815-817, Seventh International Conference (Jun. 18-21, 2001). |
Halopenen, I. et al., “Smart Laminated Glasses for Regulation of Lighting,” Glass Processing Days, Conference Proceedings, pp. 324-326, Sixth International Conference (Jun. 13-16, 1999). |
Srivastava, J. et al., “Synthesis of Polyacrylic Acid Based Thermochromic Polymers,” Proc. of SPIE, vol. 5062, pp. 111-115 (2003). |
Kojima, K. et al., “Pressure and Temperature Effects on Octahedral-Tetrahedral Equilibria in Pyridine Solutions of Some Cobalt(II) Halides,” Bull. Chem. Soc. Jpn., vol. 56, No. 3, pp. 684-688 (Mar. 1983). |
Griffiths, T.R. et al., “Effects of Cations upon Absorption Spectra Part 4.-Octahedral-Tetrahedral Equilibria between Chloro-nickel(II) Complexes in Ethylene Glycol and Glycerol,” Trans. Faraday Soc. 65, pp. 3179-3186 (1969). |
Griffiths, T.R. et al., “Effects of Cations upon Absorption Spectra Part 2.-Formation of Tetrahedral Tetrachloronickelate(II) in Aqueous Solution,” Trans. Faraday Soc., 65, pp. 1727-1733 (1969). |
Gill, Naida S. et al., “Complex Halides of the Transition Metals. Part I. Tetrahedral Nickel Complexes,” J. Chem. Soc., pp. 3397-4007 (1959). |
Sunamoto, J. et al., “Solvochromism and Thermochromism of Cobalt(II) Complexes Solubilized in Reversed Micelles,” Bulletin of the Chemical Society of Japan, vol. 51, No. 11, pp. 3130-3135 (Nov. 1978). |
Marinkovic, M. et al., “Thermochromic complex compounds in phase change materials: Possible application in an agricultural greenhouse,” Solar Energy Materials and Solar Cells, 51, pp. 401-411 (1998). |
Arutjunjan, R.E. et al., “Thermochromic Glazing for ‘Zero Net Energy’ House,” Glass Processing Days, Conference Proceedings, pp. 299-301 , Eighth International Conference (Jun. 15-18, 2003). |
Rozova, K.B. et al., Abstract for “Sun screening thermochromic glazing materials,” TsNIIEP, USSR. Svetotekhnika (1986), (10), 12-14. CODEN: SVETAG ISSN: 0039-7067. Journal written in Russian. CAN 107:30324 AN 1987:430324 CAPLUS. |
Greenberg, C., “Chromogenic Materials (Thermochromic),” Kirk-Othmer Encyclopedia of Chemical Technology 4th Edition, vol. 6, pp. 337-343, John Wiley & Sons (2000). |
Sone, K. et al., Inorganic Thermochromism, pp. 1-71, Springer-Verlag (1987). |
Angell, C.A., “Octahedral-Tetrahedral Coordination Equilibria of Nickel (II) and Copper (II) in Concentrated Aqueous Electrolyte Solutions,” Journal of the American Chemical Society, 88 (22), pp. 5192-5198 (Nov. 20, 1966). |
Day, J.H., “Thermochromism of Inorganic Compounds,” Chemical Reviews, vol. 68, No. 6, pp. 649-657 (Nov. 25, 1968). |
Scaife, D.E. et al., “Influence of Temperature on Some Octahedral-Tetrahedral Equilibria in Solution,” Inorganic Chemistry, vol. 6, No. 2, pp. 358-365 (Feb. 1967). |
Sunamoto, J. et al., “Formation of Polynuclear Cupric Halides in Cationic Reversed Micelles,” Inorganic Chemistry, vol. 19, No. 12, pp. 3668-3673 (1980). |
Sunamoto, J. et al., “Reversed Micelles to Mimic the Active Site of Metalloenzymes,” Inorganica Chimca Acta, 92, pp. 159-163 (1984). |
Katzin, L.I., “Energy Value of the Octahedral-Tetrahedral Coordination Change,” The Journal of Chemical Physics, vol. 35, No. 2, pp. 467-472 (Aug. 1961). |
Sestili, L. et al., “Formation Equilibria of Pseudotetrahedral Co(II) Halogenocomplexes in Acetonitrile,” J. Inorg. Nucl. Chem., No. 32, pp. 1997-2008 (1970). |
Kirk-Othmer Encyclopedia of Chemical Technology Third Edition, vol. 6 “Chromogenic Materials (Electro-, Thermo) Electrochromic and Thermochromic,” pp. 129-142, John Wiley & Sons (1979). |
Long, G.J. et al., “Transition Metal Chemistry of Quinuclidinone-Containing Ligands. III. Electronic and Structural Properties of Several Transition Metal Complexes Containing trans-2-(2′-Quinolyl)methylene-3-quinuclidinone,” Inorganic Chemistry, vol. 13, No. 2, pp. 270-278 (XP-002465696) (1974). |
Kuroiwa, K. et al., “Heat-Set Gel-like Networks of Lipophilic Co(II) Triazole Complexes in Organic Media and Their Thermochromic Structural Transitions,” Journal of the American Chemical Society, vol. 126, pp. 2016-2021 (XP-002465697) (2004). |
Weber, Michael F. “Giant Birefringent Optics in Multilayer Polymer Mirrors”, Science, vol. 287, pp. 2451-2456. (2000). |
Number | Date | Country | |
---|---|---|---|
20130229702 A1 | Sep 2013 | US |
Number | Date | Country | |
---|---|---|---|
61600767 | Feb 2012 | US |