Patent Application
20100316886
1. Field of the Invention
This invention relates generally to vehicle transparencies and, in one particular embodiment, to an aircraft transparency having solar control properties.
2. Technical Considerations
Aircraft transparencies, such as aircraft cockpit or cabin windows, are typically made of one or more polymeric substrates mounted in a framework. Polymer substrates are lighter in weight than glass substrates, which decreases the overall weight of the aircraft, which in turn saves fuel. Also, these polymer substrates have higher fracture toughness than glass substrates providing improved safety. These conventional cabin windows allow passengers to see out of the aircraft and allow sunlight to enter the cabin. However, the transmission of solar energy through the cabin window can increase the temperature inside the cabin, which can increase the load on the aircraft's air conditioning system.
In an effort to decrease the heat load transmitted through conventional cabin windows, various shading devices have been developed. These can range from simple devices, such as an opaque sun shade that can be raised and lowered, to complex devices, such as electrochromic devices that darken upon the application of an electrical potential. However, these shading devices also have some drawbacks. If a passenger uses the sun shade or darkens the electrochromic device to cut down on the heat transfer into the cabin, the passenger can no longer enjoy the view out of the window. Also, solar energy passing through the cabin window can heat up or damage the components of the electrochromic device.
Therefore, it would be advantageous to provide an aircraft transparency, such as an aircraft cabin window, that has improved solar control properties compared to prior aircraft transparencies but that does not substantially adversely impact upon a passenger's view out of the aircraft transparency.
An aircraft transparency comprises a first polymeric ply having a first major surface and second major surface, a second polymeric ply having a third major surface and a fourth major surface, and a coating stack applied over at Least a portion of one or more of the major surfaces. The plies can be spaced apart and can be, for example, stretched acrylic. The coating stack can include a functional coating or portion having one or more functions, such as but not limited to, solar control, electromagnetic shielding, anti-static, heating, de-icing, anti-reflective, anti-glint, or anti-glare, just to name a few. For example, the functional coating can be a solar control coating having three or more metallic layers.
Another aircraft transparency comprises a first stretched acrylic ply having a first major surface and second major surface and a second stretched acrylic ply having a third major surface and a fourth major surface. The plies can be spaced apart. A coating stack having solar control properties is applied over at least a portion of one or more of the major surfaces. The coating stack comprises a first primer layer formed over at least a portion of one of the major surfaces. The first primer layer can comprise an epoxy amino siloxane-containing material or any adhesion promoter with intermediate mechanical properties between the substrate and the overlying layer(s). Examples also include polysiloxane materials or UV-cured acrylic materials. A solar control coating is formed over at least a portion of the first primer layer, the solar control coating comprising at least three metallic silver layers. A protective coating (e.g., adhesion promoting coating) is formed over at least a portion of the solar control coating, the protective coating comprising silica and alumina. A topcoat can be formed over at least a portion of the protective coating and comprises a polysiloxane material. Alternatively, the topcoat can be absent. An overcoat is formed over at least a portion of the topcoat and comprises a diamond-like carbon type coating, such as a silicon oxycarbide coating.
A method of making an aircraft transparency comprises the steps of: providing a first stretched acrylic ply having a first major surface and a second major surface; providing a second stretched acrylic ply having a third major surface and a fourth major surface; and providing a coating stack having solar control properties over at least a portion of one or more of the major surfaces. The coating stack comprises: a first primer layer formed over at least a portion of one of the major surfaces, the first primer layer comprising an epoxy amino siloxane-containing material; a solar coating formed over at least a portion of the first primer layer, the solar control coating comprising at least three metallic silver layers; a protective coating formed over at least a portion of the solar control coating, the protective coating comprising silica and alumina; an optional topcoat formed over at least a portion of the protective coating and comprising a polysiloxane material; and an overcoat formed over at least a portion of the topcoat and comprising a diamond-like carbon type coating.
A further aircraft transparency comprises a stretched acrylic ply having a first major surface and a second major surface. A topcoat is formed over at least a portion of at least one major surface of the ply, for example the outer surface, and comprises a polysiloxane material, for example having a hybrid copolymer. An overcoat is formed over at least a portion of the topcoat and comprises a silicon oxycarbide coating. For example, the topcoat can comprise a polysiloxane polymer comprising the reaction product of: (a) a hybrid copolymer comprising (i) a first monomer comprising a hydroxy functional organoacrylate and (ii) a second monomer comprising an organoalkoxysilane, and (b) a second material comprising an organoalkoxysilane.
The invention will be described with reference to the following drawing figures wherein like reference numbers identify like parts throughout.
As used herein, spatial or directional terms, such as “left”, “right”, “inner”, “outer”, “above”, “below”, and the like, relate to the invention as it is shown in the drawing figures. However, it is to be understood that the invention can assume various alternative orientations and, accordingly, such terms are not to be considered as limiting. Further, as used herein, all numbers expressing dimensions, physical characteristics, processing parameters, quantities of ingredients, reaction conditions, and the like, used in the specification and claims are to be understood as being modified in all instances by the term “about”. Accordingly, unless indicated to the contrary, the numerical values set forth in the following specification and claims may vary depending upon the desired properties sought to be obtained by the present invention. At the very least, and not as an attempt to limit the application of the doctrine of equivalents to the scope of the claims, each numerical value should at least be construed in light of the number of reported significant digits and by applying ordinary rounding techniques. Moreover, all ranges disclosed herein are to be understood to encompass the beginning and ending range values and any and all subranges subsumed therein. For example, a stated range of “1 to 10” should be considered to include any and all subranges between (and inclusive of) the minimum value of 1 and the maximum value of 10; that is, all subranges beginning with a minimum value of 1 or more and ending with a maximum value of 10 or less, e.g., 1 to 3.3, 4.7 to 7.5, 5.5 to 10, and the like. Further, as used herein, the terms “formed over”, “deposited over”, or “provided over” mean formed, deposited, or provided on an underlying surface but not necessarily in direct contact with the surface. For example, a coating layer “formed over” a substrate does not preclude the presence of one or more other coating layers or films of the same or different composition located between the formed coating layer and the substrate. As used herein, the term “film” refers to a coating region of a desired or selected coating composition. A “layer” can comprise one or more “films”. A “coating” or “coating stack” can comprise one or more “layers”. As used herein, the terms “polymer” or “polymeric” include oligomers, homopolymers, copolymers, and terpolymers, e.g., polymers formed from two or more types of monomers or polymers. The terms “visible region” or “visible light” refer to electromagnetic radiation having a wavelength in the range of 380 nm to 780 nm. The terms “infrared region” or “infrared radiation” refer to electromagnetic radiation having a wavelength in the range of greater than 780 nm to 100,000 nm. The terms “ultraviolet region” or “ultraviolet radiation” mean electromagnetic energy having a wavelength in the range of 100 nm to less than 380 nm. Additionally, all documents, such as but not limited to, issued patents and patent applications, referred to herein are to be considered to be “incorporated by reference” in their entirety.
For purposes of the following discussion, the invention will be discussed with reference to use with a vehicle transparency, particularly an aircraft transparency in the form of an aircraft cabin window. However, it is to be understood that the invention is not limited to use with aircraft cabin windows but could be practiced with transparencies in any desired field, such as but not limited to, laminated or non-laminated residential and/or commercial windows, insulating glass units, and/or transparencies for land, air, space, above water and under water vehicles. Therefore, it is to be understood that the specifically disclosed exemplary embodiments are presented simply to explain the general concepts of the invention and that the invention is not limited to these specific exemplary embodiments.
A non-limiting aircraft transparency 10 (e.g., cabin window assembly or cockpit window assembly) incorporating features of the invention is illustrated in
As shown in
The frame assembly 24 is not limiting in the invention and can be of any of several types known in the art. The frame assembly 24 can include a frame that surrounds a gasket to hold the plies 12 and 18 in a spaced-apart relationship. The frame can be made of any structurally stable material, such as but not limited to, a plastic or metal, e.g., aluminum, and operates to protect the gasket material from damage and to provide additional structural stability to the transparency 10. The air gap 26, among other things, provides thermal insulation between the atmosphere external of the aircraft cabin and the atmosphere within the cabin. Non-limiting examples of suitable frame assemblies 24 are described, for example, in U.S. Pat. Nos. 6,561,460 and 6,783,099.
In the broad practice of the invention, the plies 12, 18 of the transparency 10 can be of the same or different materials and can include any desired material having any desired characteristics. For example, one or more of the plies 12, 18 can be transparent or translucent to visible light, By “transparent” is meant having visible light transmission of greater than 0% to 100%. Alternatively, one or more of the plies 12, 18 can be translucent. By “translucent” is meant allowing electromagnetic energy (e.g., visible light) to pass through, but diffusing this energy such that objects on the side opposite the viewer are not clearly visible. Examples of suitable materials for the plies 12, 18 include, but are not limited to, plastic substrates (such as acrylic polymers, such as polyacrylates; polyalkylmethacrylates, such as polymethylmethacrylates, polyethylmethacrylates, polypropylmethacrylates, and the like; polyurethanes; polycarbonates; polyalkylterephthalates, such as polyethyleneterephthalate (PET), polypropyleneterephthalates, polybutyleneterephthalates, and the like; polysiloxane-containing polymers; or copolymers of any monomers for preparing these, or any mixtures thereof); ceramic substrates; glass substrates; or combinations of any of the above. In one non-limiting embodiment, both of the plies 12, 18 are made of a polymeric material, such as stretched acrylic. However, in other embodiments, one or more of the plies 12, 18 can be conventional soda-lime-silicate glass, borosilicate glass, leaded glass, low iron glass, lithium doped glass, or lithium alumina silicate glass. One or more of the glass plies can be clear glass, i.e., non-tinted or non-colored glass, or can be tinted or otherwise colored glass. The glass can be annealed, heat-treated, or chemically tempered glass. As used herein, the term “heat-treated” means tempered or at least partially tempered. The glass can be of any type, such as conventional float glass, and can be of any composition having any optical properties, e.g., any value of visible transmission, ultraviolet transmission, infrared transmission, and/or total solar energy transmission. In the non-limiting embodiment shown in
The first and second plies 12, 18 can be of any desired dimensions, e.g., length, width, shape, or thickness. While the dimensions of the transparency 10 are not limiting to the invention, in one non-limiting embodiment for aircraft window assemblies having overall dimensions of approximately 20 inches (51 cm) in width by 25 inches (64 cm) in height and an overall thickness in the range of 1.5 to 2.5 inches (3.8 to 6.4 cm), an air gap 26 thickness in the range of 1.0 inch (2.54 cm) to 2.0 inches (5.08 cm) is acceptable.
The plies 12, 18 can be of any thickness. However, as can be appreciated by those skilled in the art, increasing the thickness of plies 12, 18, beyond that needed to withstand the rigors of flight, undesirably increases the weight of the transparency 10. For example and without limiting the present invention, for many applications, a ply thickness ranging from 0.20 to 0.40 inch (0.51 to 1.02 cm) is acceptable to withstand the rigors of flight. In one particular non-limiting embodiment, the plies 12, 18 are stretched acrylic and have a thickness ranging from 0.31 to 0.40 inch (0.79 to 1.02 cm).
The coating stack 30 having solar control properties is deposited over at least a portion of a major surface of one of the plies 12, 18. In the non-limiting embodiment shown in
The primer layer 32 aids in adhering the solar control coating 36 to the substrate (ply) 12 and also provides an intermediate stiffness between the substrate, e.g., stretched acrylic ply 12, and the subsequently applied coatings. Suitable primer materials include, but are not limited to, siloxane based primers, organosilane primers, epoxy amino siloxane primers, polysiloxane primers, and acrylic primers. Examples of suitable primer materials are described in U.S. Pat. Nos. 5,939,188; 4,670,350; 4,816,288; 4,725,501; 5,994,452; 6,110,327; and 5,776,548. The primer layer 32 can be applied in any conventional manner, such as by flow coating. In one particular non-limiting embodiment, the primer layer 32 comprises a polysiloxane or an epoxy amino siloxane material and has a thickness in the range of 0.1 to 10 microns, such as 0.5 to 8 microns, such as 1 to 5 microns, such as 1 to 3microns, such as 1 to 2 microns. Alternatively, for some substrates, such as polyurethane, the primer layer 32 can be eliminated.
An optional first protective coating 34 can be applied over the primer layer 32. The protective coating 34 can help protect the solar control coating 36 from mechanical and/or chemical attack by any materials leaching from the primer layer 32 or caused by any subsequent processing steps. The protective coating 34 can be of any desired material or mixture of materials, such as but not limited to, one or more inorganic materials. Examples of suitable materials include, but are not limited to, metal oxides, silicon oxides, aluminum oxides, aluminosilicates, silicon nitrides, silicon carbides, and silicon oxycarbides, just to name a few. In one exemplary embodiment, the protective coating 34 can include one or more metal oxide materials, such as but not limited to, oxides of zirconium, aluminum, silicon, or mixtures thereof. For example, the protective coating 34 can be a single coating layer comprising in the range of 0 wt. % to 100 wt. % alumina and/or 0 wt. % to 100 wt. % silica and/or 0 wt. % to 100 wt. % zirconium oxide. For example, the protective coating can include silica and alumina having, for example, 1 wt. % to 99 wt. % silica and 99 wt. % to 1 wt. % alumina, such as at least 70 wt. % silica and 30 wt. % or less alumina, such as at least 75 wt. % silica, such as at least 80 wt. % silica, such as at least 85 wt. % silica. In one particular non-limiting embodiment, the protective coating 34 comprises 85 wt. % silica and 15 wt. % alumina. Other materials, such as aluminum, chromium, hafnium, yttrium, nickel, boron, phosphorous, titanium, zirconium, and/or oxides thereof, can also be present, for example, to adjust the refractive index of the protective coating 34. In one non-limiting embodiment, the refractive index of the protective coating 34 can be in the range of 1 to 3, such as 1 to 2, such as 1.4 to 2, such as 1.4 to 1.8.
In one non-limiting embodiment, the protective coating 34 comprises a combination of silica and alumina having a thickness in the range of 5 nm to 5,000 nm, such as 5 nm to 3,000 nm, such as 5 nm to 2,000 nm, such as 5 nm to 1,000 nm, such as 10 nm to 500 nm, such as 20 nm to 300 nm, such as 50 nm to 300 nm, e.g., 50 nm to 200 nm, such as 50 nm to 150 nm, such as 50 nm to 120 nm, such as 60 nm to 120 nm, such as 70 nm to 120 nm, such as 70 nm to 100 nm, such as 70 nm to 80 nm. In a particular non-limiting embodiment, the protective coating can have a thickness of at least 50 nm, such as at least 60 nm, such as at least 70 nm, such as at least 75 nm, such as at least 100 nm, such as at least 110 nm, such as at least 120 nm, such as at least 150 nm, such as at least 200 nm.
In another non-limiting embodiment, the protective coating 34 comprises a multi-layer structure, e.g., a first layer with at least one second layer formed over the first layer. In one specific non-limiting embodiment, the first layer comprises alumina or a mixture or alloy comprising alumina and silica. For example, the first layer can be greater than 5 wt. % alumina, such as greater than 10 wt. % alumina, such as greater than 15 wt. % alumina, such as greater than 30 wt. % alumina, such as greater than 40 wt. % alumina, such as 50 wt. % to 70 wt. % alumina, such as in the range of 70 wt. % to 100 wt. % alumina and 30 wt. % to 0 wt. % silica, such as greater than 90 wt. % alumina, such as greater than 95 wt. % alumina. In one non-limiting embodiment, the first layer comprises all or substantially all alumina. In one non-limiting embodiment, the first layer can have a thickness in the range of greater than 0 nm to 1 micron, such as 5 nm to 10 nm, such as 10 nm to 25 nm, such as 10 nm to 15 nm.
The second layer can comprise silica or a mixture or alloy comprising silica and alumina. For example, the second layer can comprise a silica/alumina mixture having greater than 40 wt. % silica, such as greater than 50 wt. % silica, such as greater than 60 wt. % silica, such as greater than 70 wt. % silica, such as greater than 80 wt. % silica, such as in the range of 80 wt. % to 90 wt. % silica and 10 wt. % to 20 wt. % alumina, e.g., 85 wt. % silica and 15 wt. % alumina. In one non-limiting embodiment, the second layer can have a thickness in the range of greater than 0 nm to 2 microns, such as 5 nm to 500 nm, such as 5 nm to 200 nm, such as 10 nm to 100 nm, such as 30 nm to 50 nm, such as 35 nm to 40 nm. In another non-limiting embodiment, the second layer can have a thickness in the range of greater than 0 nm to 1 micron, such as 5 nm to 10 nm, such as 10 nm to 25 nm, such as 10 nm to 15 nm. In another non-limiting embodiment, the protective coating 34 can be a bilayer formed by one metal oxide-containing layer (e.g., a silica and/or alumina-containing first layer) formed over another metal oxide-containing layer (e.g., a silica and/or alumina-containing second layer). The individual layers of the multi-layer protective coating can be of any desired thickness. Non-limiting examples of suitable protective coatings are described, for example, in U.S. patent application Ser. Nos. 10/007,382; 10/133,805; 10/397,001; 10/422,094; 10/422,096; and 10/422,096.
The protective coating 34 can be deposited by any conventional method, such as but not limited to, conventional chemical vapor deposition (CVD) and/or physical vapor deposition (PVD) methods. Examples of CVD processes include spray pyrolysis. Examples of PVD processes include electron beam evaporation and vacuum sputtering (such as magnetron sputter vapor deposition (MSVD)). Other coating methods could also be used, such as but not limited to, sol-gel deposition. In one non-limiting embodiment, the protective coating can be deposited by MSVD.
A solar control coating 36 is deposited over the primer layer 32 (or over the protective coating 34, if present). As used herein, the term “solar control coating” refers to a coating comprised of one or more layers or films that affect the solar properties of the coated article, such as but not limited to, the amount of solar radiation, for example, visible, infrared, or ultraviolet radiation, reflected from, absorbed by, or passing through the coated article; shading coefficient; emissivity, etc. The solar control coating 36 can block, absorb or filter selected portions of the solar spectrum, such as but not limited to the IR, UV, and/or visible spectrums. Examples of solar control coatings that can be used in the practice of the invention are found, for example but not to be considered as limiting, in U.S. Pat. Nos. 4,898,789; 5,821,001; 4,716,086; 4,610,771; 4,902,580; 4,716,086; 4,806,220; 4,898,790; 4,834,857; 4,948,677; 5,059,295; and 5,028,759, and also in U.S. patent application Ser. No. 09/058,440.
In one non-limiting embodiment, the solar control coating 36 includes one or more metallic films positioned between pairs of dielectric layers. The solar control coating 36 can be a heat and/or radiation reflecting coating and can have one or more coating layers or films of the same or different composition and/or functionality. For example, the solar control coating 36 can be a single-layer coating or a multi-Layer coating and can include one or more metals, non-metals, semi-metals, semiconductors, and/or alloys, compounds, compositions, combinations, or blends thereof. For example, the solar control coating 36 can be a single-layer metal oxide coating, a multiple-layer metal oxide coating, a non-metal oxide coating, a metallic nitride or oxynitride coating, a non-metallic nitride or oxynitride coating, or a multiple-layer coating comprising one or more of any of the above materials. In one non-limiting embodiment, the solar control coating 36 can be a doped metal oxide coating.
Non-limiting examples of suitable solar control coatings for use with the invention are commercially available from PPG Industries, Inc. of Pittsburgh, Pa. under the SUNGATE® and SOLARBAN® families of coatings. Such coatings typically include one or more anti-reflective coating films comprising dielectric or anti-reflective materials, such as metal oxides or oxides of metal alloys, which are transparent to visible light. These coatings also include one or more infrared reflective films comprising a reflective metal, e.g., a noble metal such as gold, copper or silver, or combinations or alloys thereof, and can further comprise a sacrificial primer film or barrier film, such as titanium, as is known in the art, located over and/or under the metal reflective layer. The solar control coating 36 can have any desired number of infrared reflective films, such as but not limited to, 1 to 8 infrared reflective films. In one non-limiting embodiment, the solar control coating 36 can have 1 or more metallic silver layers, e.g., 2 or more silver layers, e.g., 3 or more silver layers, such as 4 or more silver layers, such as 5 or more silver layers, such as 6 or more silver layers. A non-limiting example of a suitable solar control coating having three silver layers is disclosed in U.S. patent application Ser. No. 10/364,089 (Publication No. 2003/0180547 A1).
The solar control coating 36 can be deposited by any conventional method, such as but not limited to, conventional chemical vapor deposition (CVD) and/or physical vapor deposition (PVD) methods. Examples of CVD processes include spray pyrolysis. Examples of PVD processes include electron beam evaporation, RF plasma deposition, and vacuum sputtering (such as magnetron sputter vapor deposition (MSVD)). Other coating methods could also be used, such as but not limited to, sol-gel deposition. In one non-limiting embodiment, the coating can be deposited by MSVD.
A non-limiting solar control coating 36 suitable for the invention is shown in
In the illustrated exemplary embodiment shown in
The second film 54 can be a zinc-containing film, such as zinc oxide. The zinc oxide film can be deposited from a zinc cathode that includes one or more other materials to improve the sputtering characteristics of the cathode. For example, the zinc cathode can include a small amount (e.g., up to 10 wt. %) of tin to improve sputtering. In which case, the resultant zinc oxide film would include a small percentage of tin oxide, e.g., up to 10 wt. % tin oxide. An oxide coating sputtered from a zinc cathode having up to 10 wt. % tin is referred to herein as a “zinc oxide” film even though some tin oxide may be present. The second film 54 can have a thickness in the range of 10 Å to 200 Å, such as 20 Å to 200 Å, such as 30 Å to 200 Å, 40 Å to 150 Å, e.g., 50 Å to 100 Å, such as 60 Å to 100 Å, such as 60 Å to 80 Å, such as 70 Å to 80 Å, such as 73 Å.
A first heat and/or radiation reflective film or layer 56 is deposited over the first dielectric layer 50. The first reflective layer 56 includes a reflective metal, such as but not limited to, metallic gold, copper, silver, or mixtures, or alloys thereof. In one embodiment, the first reflective layer 56 comprises a metallic silver layer having a thickness in the range of 25 Å to 300 Å, e.g., 50 Å to 300 Å, e.g., 50 Å to 200 Å, such as 70 Å to 150 Å, such as 70 Å to 100 Å, such as 80 Å to 100 Å, such as 90 Å to 100 Å such as 90 Å.
A first sacrificial primer film 58 is deposited over the first reflective layer. The first sacrificial primer film 58 can be an oxygen-capturing material, such as titanium, that can be sacrificial during the deposition process to prevent degradation or oxidation of the first reflective layer 56 during the sputtering process or subsequent heating processes. The oxygen-capturing material can be chosen to oxidize before the material of the first reflective layer 56. If titanium is used as the first primer film 58, the titanium would preferentially oxidize to titanium dioxide before oxidation of the underlying silver layer. In one embodiment, the first primer film 58 is titanium having a thickness in the range of 5 Å to 50 A, e.g., 10 Å to 40 Å, e.g., 15 Å to 25 Å, e.g., 15 Å to 20 Å, e.g., 15 Å.
A second dielectric layer 60 is deposited over the first reflective layer 56 (e.g., over the first sacrificial primer film 58). The second dielectric layer 60 comprises one or more metal oxide or metal alloy oxide-containing films, such as those described above with respect to the first dielectric layer. In the illustrated non-limiting embodiment, the second dielectric layer 60 includes a first 62, such as a metal oxide film, e.g., a zinc oxide film deposited over the first sacrificial primer film 58. A second film 64, such as a metal alloy oxide film, e.g., a zinc stannate film, is deposited over the first zinc oxide film 62. A third film 66, such as a metal oxide film, e.g., another zinc/tin oxide layer, is deposited over the zinc stannate layer to form a multi-film second dielectric layer 60. In one non-limiting embodiment, the zinc oxide films of the second dielectric layer can each have a thickness in the range of about 10 Å to 200 Å, e.g., 20 Å to 150 Å, e.g., 30 Å to 100 Å, e.g., 40 Å to 80 Å, e.g., 50 Å to 80 Å, e.g., 60 Å to 80 Å, e.g., 70 Å to 80 Å, such as 73 Å. The metal alloy oxide layer (zinc stannate) can have a thickness in the range of 100 Å to 1000 Å, e.g., 200 Å to 1000 Å, e.g., 300 Å to 800 Å, e.g., 500 Å to 800 Å, e.g., 600 Å to 800 Å, e.g., 600 Å to 700 Å; e.g., 631 Å.
A second heat and/or radiation reflective layer 68 is deposited over the second dielectric layer 60. The second reflective layer 68 can include any one or more of the reflective materials described above with respect to the first reflective layer 56. In one non-limiting embodiment, the second reflective layer 68 comprises silver having a thickness in the range of 25 Å to 200 Å, e.g., 50 Å to 150 Å, e.g., 60Å to 100 Å, e.g., 70 Å to 100 Å, e.g., 80 Å to 90 Å, e.g., 83 Å.
A second sacrificial primer film 70 can be deposited over the second reflective layer 68. The second sacrificial primer film 70 can be any of the materials described above with respect to the first primer film 32. In one non-limiting embodiment, the second primer film 70 includes titanium having a thickness in the range of about 5 Å to 50 Å, e.g., 10 Å to 25 Å, e.g., 15 Å to 25 Å, e.g., 15 Å to 20 Å, e.g., 15 Å.
A third dielectric layer 72 is deposited over the second reflective layer 68 (e.g., over the second sacrificial primer film 70). The third dielectric layer 72 can also include one or more metal oxide or metal alloy oxide-containing layers, such as discussed above with respect to the first and second dielectric layers. In one non-limiting embodiment, the third dielectric layer 72 is a multi-film layer similar to the second dielectric layer 60. For example, the third dielectric layer 72 can include a first layer 74, such as a metal oxide layer, e.g., a zinc oxide layer, a second layer 76, such as a metal alloy oxide-containing layer, e.g., a zinc stannate layer, and a third layer 78, such as a metal oxide layer, e.g., another zinc oxide layer. In one non-limiting embodiment, the zinc oxide films of the third dielectric layer 72 can each have a thickness in the range of about 10 Å to 200 Å, e.g., 20 Å to 150 Å, e.g., 30 Å to 100 Å, e.g., 40 Å to 80 Å, e.g., 50 Å to 80 Å, e.g., 60 Å to 80 Å, e.g., 70 Å to 80 Å, e.g., 73 Å. The metal alloy oxide layer (zinc stannate) can have a thickness in the range of 100 Å to 1000 Å, e.g., 200 Å to 1000 Å, e.g., 300 Å to 800 Å, e.g., 500 Å to 800 Å, e.g., 600 Å to 80 Å, e.g., 600 Å to 700 Å, e.g., 631 Å.
A third heat and/or radiation reflective layer 80 is deposited over the third dielectric layer 72. The third reflective layer 80 can be of any of the materials discussed above with respect to the first and second reflective layers. In one non-limiting embodiment, the third reflective layer 80 comprises silver having a thickness in the range of 25 Å to 200 Å, e.g., 50 Å to 150 Å, e.g., 60 Å to 100 Å, e.g., 70 Å to 100 Å, e.g., 80 Å to 90 Å, e.g., 83 Å.
A third sacrificial primer film 82 is deposited over the third reflective layer 80. The third primer film 82 can be of any of the primer materials described above with respect to the first or second primer films. In one non-limiting embodiment, the third sacrificial primer film 82 is titanium and has a thickness in the range of 5 Å to 50 Å, e.g., 10 Å to 25 Å, e.g., 15 Å to 20 Å, e.g., 15 Å.
A fourth dielectric layer 84 is deposited over the third reflective layer 80 (e.g., over the third sacrificial primer film 82). The fourth dielectric layer 84 comprises one or more metal oxide or metal alloy oxide-containing layers, such as those discussed above with respect to the first, second, or third dielectric layers. In one non-limiting embodiment, the fourth dielectric layer 84 is a multi-film layer having a first layer 86, such as a metal oxide layer, e.g., a zinc oxide layer, deposited over the third primer film 82, and a second layer 88, such as a metal alloy oxide layer, e.g., a zinc stannate layer, deposited over the zinc oxide layer. The zinc oxide layer 86 can have a thickness in the range of 10 Å to 200 Å, such as 20 Å to 200 Å, such as 30 Å to 200 Å, 40 Å to 150 Å, e.g., 50 Å to 100 Å, such as 60 Å to 100 Å, such as 60 Å to 80 Å, such as 70 Å to 80 Å, such as 73 Å. The zinc stannate layer 88 can have a thickness in the range of 100 Å to 1,000 Å, such as 100 Å to 500 Å, such as 150 Å to 500 Å, e.g., 200 Å to 500 Å, e.g., 300 Å to 400 Å, e.g., 376 Å.
As shown in
An optional second primer layer 40 can be applied over the protective coating 38. The optional second primer layer 40 can be the same as described below for the first primer layer 32. In one particular non-limiting embodiment, the second primer layer 40 comprises an epoxy amino siloxane material and has a thickness in the range of 0.1 to 10 microns, such as 0.5 to 8 microns, such as 1 to 7 microns, such as 1 to 5 microns, such as 1 to 3 microns.
A topcoat 42 is applied over the protective coating 38 (or over the optional second primer layer 40, if present). The topcoat 42 provides abrasion resistance and/or craze resistance to the substrate 12. In one non-limiting embodiment, the topcoat 42 is a polysiloxane material. Suitable topcoat materials are disclosed in WO 2007/064792 A2 and U.S. Pat. Nos. 5,693,422; 6,106,605; 6,180,248; 5,401,579; and 6,469,119. Other suitable topcoat materials are commercially available from Advanced Materials and Coating Specialties under the names LensShield 500, 501, 503, 510, and 514. The topcoat 42 can have a thickness in the range of 1 to 10 microns, such as 2 to 8 microns, such as 3 to 7 microns, such as 4 to 6 microns, such as 4 to 5 microns. The topcoat can be applied by any conventional method, such as by flow coating.
The material for the topcoat 42 can incorporate a polymer having both polysiloxane-based hard coating functionality as well as more flexible organopolymeric functionality, such as but not limited to acrylic or epoxy functionality. Exemplary topcoat material can be made as follows and as described in the following examples.
A hybrid copolymer is prepared having at least two different monomer units. In one particular non-limiting embodiment, the hybrid copolymer is a copolymer prepared from the reaction product of (i) a first monomer comprising a hydroxy-functional organoacrylate and (ii) a second monomer comprising an organofunctional alkoxysilane, such as a silicon alkoxide with a polymerizable group.
In one non-limiting embodiment, the first monomer comprises a hydroxyacrylate and/or a hydroxyalkylacrylate. The alkyl portion of the hydroxyalkylacrylate can be generally represented by the formula CnH2n+1 where n is in the range of 1-20, such as 1-10 such as 1-5. Specific examples of the first monomer include, but are not limited to hydroxyrmethylacrylate, hydroxyethylacrylate, and hydroxypropylacrylate.
The second monomer is an alkoxide, such as an organofunctional alkoxysilane, such as an organofunctional trialkoxysilane. The alkoxide may contain alkyl or aryl groups. Silanes of the general formula RxSi(OR′)4-x can be used, where R is an organic radical, R′ is a low molecular weight alkyl radical, and x is in the range of 1 to 4. The organic radical of R can be, vinyl, methoxyethyl, 3-glycidoxypropyl, or 3-methacryloxypropyl, just to name a few. In one non-limiting embodiment, the second monomer is a trialkoxysilane of the general formula RSi(OR′)3, where R is a short to medium chain length organic group capable of undergoing polymerization such as vinyl, 3-glycidoxypropyl, or 3-methacryloxypropyl. In one particular embodiment, the second monomer is selected from methacryloxypropyltrimethoxysilane or vinyltrimethoxysilane.
The first and second monomers are combined with an appropriate catalyst, such as azobisisobutyrolnitrile (AIBN), to form a hybrid copolymer. In the broad practice of the invention, the first and second monomers can be combined in any ratio, such as 1 wt. % to 99 wt. % of the first monomer to 99 wt. % to 1 wt. % of the second monomer based on the total weight of the combined monomers, such as 40 wt. % to 90 wt. % of the first monomer, such as 50 wt. % to 80 wt. % of the first monomer, such as 60 wt. % to 80 wt. % of the first monomer, such as 70 wt. % to 80 wt. % of the first monomer, such as 75 wt. % of the first monomer. The hybrid copolymer can be polymerized by free radical polymerization.
The second material is reacted in the presence of the hybrid copolymer, for example by condensation polymerization, to form a polysiloxane polymer. This allows the second material to react with the hybrid copolymer as well as to polymerize with itself, for example by condensation polymerization, providing a mechanism for direct chemical bonding between the two polymeric components. The second material can comprise an alkoxide, such as an organoalkoxysilane. The organoalkoxysilane may be an alkylalkoxysilane or organofunctional alkoxysilane, such as an organofunctional trialkoxysilane, or a mixture thereof. In one non-limiting embodiment, the second material is a trialkoxysilane of the general formula RSi(OR′)3, where R is a short to medium chain length organic group such as alkyl, vinyl, phenyl, 3-glycidoxypropyl, or 3-methacryloxypropyl. In one particular embodiment, the second material is methyltrimethoxysilane.
The hybrid copolymer and the second material can be reacted by any known technique, such as a conventional condensation reaction. Examples of conventional techniques are described in U.S. Pat. Nos. 5,693,422; 5,401,579; 6,106,605; 6,180,248; and 6,469,119. The hybrid copolymer and second material can be combined in any desired ratio, such as 1 wt. % to 99 wt. % of the hybrid copolymer to 99 wt. % to 1 wt. % of the second material based on the total weight of the hybrid copolymer and second material, such as 5 wt. % to 50 wt. % of the hybrid copolymer, such as 10 wt. % to 40 wt. % of the hybrid copolymer, such as 10 wt. % to 30 wt. % of the hybrid copolymer, such as 15 wt. % to 20 wt. % of the hybrid copolymer, such as 17 wt. % of the hybrid copolymer.
The resultant hybrid copolymer (i.e. the polymer formed from the reaction of the first hybrid copolymer and the second material) can be incorporated into a coating composition that provides improved scratch, abrasion, and chemical resistance, yet sufficient to survive deformation or elongation of the underlying plastic substrate without cracking or debonding. The acrylic functionality provides enhanced weatherability and improved adhesion to both acrylic and polycarbonate substrates compared to previous protective hardcoats. In the practice of the invention, forming the hybrid copolymer by copolymerizing a hydroxy-functional acrylic monomer with a trialkoxysilane provides a copolymer that can undergo further hydrolysis of the alkoxy groups, resulting in a condensation reaction with the polysiloxane matrix of the coating solution.
The hybrid copolymer need not be limited to a copolymer having two monomers but could include three or more monomers. For example, the resultant hybrid copolymer could be a terpolymer comprising a hydroxy-functional organoacrylate, a silicon alkoxide, and a non-hydroxy functional monomer, such as but not limited to methylmethacrylate or N-vinylpyrrolidone, or any such monomer that undergoes free radical polymerization. Moreover, the hybrid copolymer is not limited to alkylacrylates, but could incorporate other acrylic functional materials, such as but not limited to aromatic acrylates or halogenated acrylates, such as fluoracrylate. Also, in addition to forming organic/inorganic hybrid copolymers by co-polymerizing a (hydroxyfunctional) organic acrylate or methacrylate monomer with an acrylate or methacrylate functional silicon alkoxide, such organic-inorganic hybrid copolymers can be formed by combining any organic monomer with any silicon alkoxide compound that contains a polymerizable group that can undergo the same kind of polymerization reaction. 1,3-bis(3-methacryloxypropyl)tetrakis (trimethylsiloxy)disiloxane is a similar methacryloxypropyl-trimethylsiloxy compound. For example, vinyl, alkenyl, and styryl functional organosilanes such as vinyltrimethoxysilane, vinyltriethoxysilane, p-(t-butyldimethylsiloxy)stryrene, and vinyl terminated polydimethylsiloxane prepolymer can be copolymerized with organic monomers by thermal or UV initiated free radical polymerization, as can the acrylic and methacrylic functional organosilanes. Also, epoxy and glycidoxy-functional silicon alkoxides, bis[methyldimethoxysilyl)propyl]polypropyleneoxide, and epoxy terminated polydimethylsiloxane prepolymer can be co-polymerized with organic epoxides by cationic UV polymerization or amine addition polymerization. Further, monomers capable of undergoing condensation polymerization can be used to form hybrid polyimide, polyamide and urethane copolymers with the appropriate amine functional silicon compounds, such as 1,3-bis(aminopropyl)tetramethyldisiloxane. Monomers capable of undergoing substitution polymerization can be combined with silicon compounds such as bis(trimethylsilyl)bisphenol A to form hybrid copolymers by substitution polymerization. As recognized by those skilled in the art, various techniques for purifying the hybrid copolymer for, example by precipitation or fractionation, can be employed to obtain hybrid copolymer materials with a narrower distribution of properties and thereby affecting the properties of the coating composition.
The following examples illustrate various non-limiting embodiments of a topcoat material. However, it is to be understood that the invention is not limited to the specific examples.
The following ingredients were combined in a glass jar: 70 grams (g) of Dowanol PM glycol ether, 22.5 g of 2-hydroxypropylacrylate, 7.5 g of gamma-methacryloxypropyltrimethoxysilane, and 0.06 g of azobisisobutyrolnitrile (AIBN). The solution was outgassed for 5 minutes under vacuum, purged with nitrogen gas via a bubbler for 5 minutes, and placed in a nitrogen filled oven at 180° F. overnight. The mixture was shaken several times over the first hour.
45 g of 2-hydroxypropylacrylate, 15 g of gamma-methacryloxypropyltrimethoxysilane, and 0.12 g of azobisisobutyrolnitrile (AIBN) were added to 140 g of Dowanol PM glycol ether in a glass jar containing a magnetic stir bar. The jar was placed in an ultrasonic bath for five minutes to assist dissolution of the AIBN, outgassed in a vacuum dessicator for 15 minutes, and transferred to a nitrogen-purged reaction setup consisting of a 250 milliliter (mL) 3-neck round bottom flask that was fitted with a reflux condenser, heating mantle, and nitrogen bubbler and heated to maintain approximately 80° C. overnight under nitrogen. The reaction mixture was allowed to cool to room temperature.
45 g of hydroxypropylacrylate (mixture of isomers), 15 g of gamma-methacryloxypropyltrimethoxysilane, and 0.12 g of azobisisobutyrolnitrile (AIBN) were added to 140 g of Dowanol PM glycol ether in a glass jar containing a magnetic stir bar. The solution was stirred for 2-3 minutes to dissolve most of the AIBN, placed in an ultrasonic bath for five minutes, degassed in a vacuum dessicator for 30 minutes, and transferred to a nitrogen-purged reaction setup consisting of a 250 mL 3-neck round bottom flask that was fitted with a reflux condenser, heating mantle, and nitrogen bubbler. After 10 minutes of vigorous nitrogen purge through the solution, heating was begun with stirring. After 45 minutes of heating, the nitrogen purge was slowed to a minimum and the temperature reached 50° C. The heat was increased so that the temperature of the reaction reached 62° C. within another 10 minutes, 78° C. within 20 minutes, at which time the exothermic reaction was in progress. The temperature reached a maximum of approximately 107-108° C. 15 minutes later, after which the exotherm subsided and the reaction mixture cooled to 70° C. After eight hours, the heat was again increased so that the reaction mixture reached 110° C. within 1 hour, at which time the heat was removed and the reaction mixture allowed to cool slightly before using to prepare a coating solution.
Azobisisobutyrolnitrile (AIBN) had been recrystallized three times from methanol one week prior to use. In a manner similar to Example 3 above, the three ingredients were combined directly into a 5000 mL 3-neck flask that was fitted with a reflux condenser, heating mantle, and nitrogen bubbler. The gamma-methacryloxypropyltrimethoxysilane was added to the hydroxypropylacrylate, which was then within 3 minutes added to the Dowanol PM glycol ether in the round bottom flask. After five minutes of stirring at room temperature, heating was begun. Twenty minutes later the temperature of the solution had reached 50° C. and 0.10 g of AIBN dissolved in 10-15 mL of Dowanol PM was added via syringe through a rubber septum. Forty minutes later the temperature of the reaction mixture had reached the maximum of 119° C. (60 minutes after start of reaction), after which it fell to 83° C. which was maintained until the total reaction time reached 16 hours. After cooling to room temperature, the copolymer product was used to prepare a polysiloxane coating solution. Material that was not used immediately was transferred to a brown glass bottle and stored in a refrigerator. After seven weeks of refrigerated storage, the room temperature viscosity of the product solution was 61.1 centipoises (cps).
Recrystallized azobisisobutyrolnitrile (AIBN) was again recrystallized one time from methanol prior to use. In a manner similar to Example 3 above, the three ingredients were combined directly into the 250 mL 3-neck flask. First the gamma-methacryloxypropyltrimethoxysilane was added to the hydroxypropylacrylate, and then the mixture of the two monomers was added with stirring to 130 g of Dowanol PM glycol ether solvent (130 g) that had been purged with nitrogen in the 3-neck flask for 2 hours. Heating was begun immediately, with the reaction solution reaching 56° C. after 24 minutes, at which time 0.10 g of AIBN was added. The reaction solution reached 117° C. by 45 minutes after the start of the reaction. At approximately 1.25 hours reaction time, the temperature had fallen to 109° F. at which time the heat was decreased to maintain a temperature of 86° C. overnight. After a total time of 16.5 hours since start of the reaction, the heat was removed to allow the product to cool to room temperature in about an hour. The product was then used to prepare a polysiloxane coating solution or transferred to a brown glass bottle for refrigerated storage. After approximately 1 week of refrigerated storage, the viscosity of the product at room temperature was 130.6 cps.
22.5 g of 2-hydroxypropyl acrylate, 7.5 g of gamma-methacryloxypropyltrimethoxysilane, and 0.06 g of dimethoxy 2-phenyl acetophenone (DMPA) were added to 70.0 g of Dowanol PM glycol ether solvent in a glass jar and placed in an ultrasonic bath until the DMPA dissolved. The solution was then outgassed for 10 minutes under vacuum followed by curing for 1 hour at room temperature under an atmosphere of nitrogen in an ELC 4001 UV cure unit. The moderately viscous solution of the copolymer product was allowed to cool to room temperature prior to use in preparing a coating solution.
Method I: In one non-limiting method, copolymer products of the type produced in Examples 1-6 were incorporated into durable abrasion resistant coating formulations as follows. In a typical preparation, 15 g of the copolymer product solution was added to 72 g of methyltrimethoxysilane. In a separate container, 15 g of methanol was combined with 44.1 g of Snowtex O aqueous colloidal silica sol (commercially available from Nissan Chemical) and 3.6 g of glacial acetic acid and 1 drop of concentrated nitric acid. The silane and copolymer mixture was slowly added into the aqueous silica solution with stirring. Stirring was continued overnight. The solution was then diluted with 125 g of 1-propanol, 0.3 g of BYK-306 (commercially available from BYK Chemie) and 0.75 g of 25% tetramethylammonium hydroxide in methanol (commercially available from Fisher Scientific).
Method II: In an alternate non-limiting method, 15 g of the copolymer products of Examples 1-6 were combined with 72 g of methyltrimethoxysilane and 45 g of NPC-ST colloidal silica sol in glycol ether PM (commercially available from Nissan Chemical). In a separate container, 30 g of deionized water was combined with 3.6 g of glacial acetic acid and 1 drop of concentrated nitric acid. The water-acid mixture was slowly added to the silane/copolymer/silica mixture with stirring, which was continued overnight. The solution was then diluted with 100 g of 1-propanol, 0.3 g of BYK-306 (commercially available from BYK Chemie) and 0.75 g of 25% tetramethylammonium hydroxide in methanol (commercially available from Fisher Scientific).
The coatings can be applied to acrylic substrates (coated or uncoated) by flow coating followed by drying in ambient air for 20-30 minutes and heat curing at 80° C. for 4 hours.
An overcoat 44 (wear-resistant coating) is applied over the topcoat 42. The overcoat 44 can be, for example, a silicon based coating, a diamond-like carbon (DLC) coating, a diamond-like carbon type coating (such as a silicon oxycarbide coating), or any such similar coating. Examples of suitable overcoat coatings are described in WO 2007/064792 A2. Other examples include DIAMONEX coatings, such as Everscan, Scanshield, AegisPlus, and DIAMONDSHIELD® coatings, commercially available from Morgan Technical Ceramics of Allentown, Pa. The overcoat 44 can have a thickness of 1 to 10 microns, such as 1 to 8 microns, such as 2 to 6 microns, such as 3 to 6 microns, such as 4 to 5 microns. The overcoat 44 can be applied by any conventional method, such as by direct ion beam deposition or RF plasma deposition.
Alternatively, the overcoat 44 can be eliminated and the topcoat 42 applied over the second protective coating 38 which is applied over the solar control coating 36. The topcoat can have a thickness, for example, in the range of 7 microns to 10 microns.
An alternative embodiment 90 of a topcoat 92 and overcoat 44 structure for the coating stack 30 is shown in
Another alternative embodiment 100 of a topcoat and overcoat structure for the coating stack 30 is shown in
The electrochromic assembly 28 (see
Another window assembly 110 is shown in
Another embodiment 114 of the invention is shown in
While various aspects of the invention have been described above, other variations are contemplated within the scope of the invention. For example but not to be considered as limiting, the topcoat 42 can be eliminated and the overcoat 44 formed on the underlying coating layers (
It will be readily appreciated by those skilled in the art that modifications may be made to the invention without departing from the concepts disclosed in the foregoing description. Accordingly, the particular embodiments described in detail herein are illustrative only and are not limiting to the scope of the invention, which is to be given the full breadth of the appended claims and any and all equivalents thereof.
This application claims priority to U.S. Application No. 61/186,465 filed Jun. 12, 2009 and also to U.S. Application No. 61/235,130 filed Aug. 19, 2009, both of which applications are herein incorporated by reference in their entirety.
| Number | Date | Country | |
|---|---|---|---|
| 61186465 | Jun 2009 | US | |
| 61235130 | Aug 2009 | US |
