This disclosure relates generally to metal oxide films. More specifically, methods for producing white appearing metal oxide films using subsurface cracking techniques are disclosed.
Metal surfaces of many consumer products are often protected with a thin film of metal oxide. The metal oxide is generally harder than the underlying metal and thus provides a protective coating for the metal. Often, the metal oxide film is formed using an anodizing process. Anodizing is an electrolytic process that increases the thickness of a natural oxide layer on the surface of metal parts. The metal part to be treated forms an anode of an electrical circuit such that the surface of the metal part is converted to a metal oxide film, also referred to as an anodic film. The anodic film can also be used for a number of cosmetic effects. For example, techniques for colorizing anodic films have been developed that can provide an anodic film with a perceived color based. A particular color can be perceived when a light of a particular range of frequencies is reflected off the surface of the anodic film.
In some cases, it can be desirable to form an anodic film having a white color. However, conventional attempts to provide white appearing anodic films have resulted in anodized films that appear to be off-white, muted grey, and yellowish white instead of a crisp appearing white that many people find appealing.
In one aspect, a method of modifying an appearance of an oxide film disposed on a substrate surface is described. The oxide film may be made of metal oxide material. The method may include forming at least one melted portion by heating the metal oxide material within a portion of the oxide film to a melting temperature of the metal oxide material. The method may further include creating several cracks within the oxide film by allowing the melted portion to cool and contract. Each of the several cracks is positioned substantially entirely beneath a top surface of the oxide film. The several cracks within the oxide film cause visible light incident a top surface of the oxide film to scatter imparting a white appearance to the oxide film.
In another aspect, a part is described. The part may include a metal substrate and a metal oxide layer. The metal substrate may include a substrate surface, the substrate surface having a mirror finish that specularly reflects substantially all visible light incident the substrate surface. The metal oxide layer disposed on the metal substrate, the metal oxide layer having a bottom surface adjacent the substrate surface and a top surface opposite the bottom surface. The metal oxide layer may include a first portion that is substantially translucent to visible light incident the top surface of the oxide layer such that at least a portion of visible light incident the top surface travels through the first portion and specularly reflects off the substrate surface. The metal oxide layer may also include a second portion having several cracks positioned beneath the top surface. Visible light incident the top surface of the oxide film diffusely reflects off the several cracks imparting a white quality to the second portion.
In another aspect, an enclosure for an electronic device is described. The enclosure may include a substrate and an oxide layer. The substrate may have several protrusions forming a first roughness. The oxide layer may be formed over the several protrusions. The oxide layer may include a first portion having several crystalline portions. A first light right ray reflected by the several crystalline structures forms a first appearance, and a second light ray absorbed by the several protrusions of a first roughness forms a second appearance. The second appearance may be different from the first appearance.
Other systems, methods, features and advantages of the embodiments will be, or will become, apparent to one of ordinary skill in the art upon examination of the following figures and detailed description. It is intended that all such additional systems, methods, features and advantages be included within this description and this summary, be within the scope of the embodiments, and be protected by the following claims.
The disclosure will be readily understood by the following detailed description in conjunction with the accompanying drawings, wherein like reference numerals designate like structural elements, and in which:
Those skilled in the art will appreciate and understand that, according to common practice, various features of the drawings discussed below are not necessarily drawn to scale, and that dimensions of various features and elements of the drawings may be expanded or reduced to more clearly illustrate the embodiments of the present invention described herein.
Reference will now be made in detail to representative embodiments illustrated in the accompanying drawings. It should be understood that the following descriptions are not intended to limit the embodiments to one preferred embodiment. To the contrary, it is intended to cover alternatives, modifications, and equivalents as can be included within the spirit and scope of the described embodiments as defined by the appended claims.
This application relates to various methods and apparatuses used for treating a metal oxide film such that the metal oxide film appears white. In some embodiments, methods involve modifying at least a portion of the metal oxide film to a crystalline form metal oxide. In some embodiments, methods involve creating cracks or small gaps within the metal oxide film and beneath a top surface of the metal oxide film. In some embodiments, methods involve creating crystalline portions combined with creating cracks. The crystalline metal oxide or cracks within the metal oxide can interact with visible light incident the top surface of the film to give the metal oxide film a white appearance. The white appearing metal oxide films are well suited for providing protective and attractive surfaces to visible portions of consumer products. For example, methods described herein can be used for providing protective and cosmetically appealing exterior portions of metal enclosures and casings for electronic devices, such as those manufactured by Apple Inc., based in Cupertino, Calif.
As used herein, the terms oxide film, oxide layer, metal oxide film, and metal oxide layer may be used interchangeably and can refer to any appropriate metal oxide material. In some embodiments, the oxide film is formed using an anodizing process and can be referred to as an anodic film or anodic layer. The metal oxide films are formed on metal surfaces of a metal substrate. The metal substrate can include any of a number of suitable metals. In some embodiments, the metal substrate includes pure aluminum or aluminum alloy. In some embodiments, suitable aluminum alloys include 1000, 2000, 5000, 6000, and 7000 series aluminum alloys.
In general, white is the color of objects that diffusely reflect nearly all visible wavelengths of light. Thus, a metal oxide film can be perceived as white when nearly all visible wavelengths of light incident a top surface of the metal oxide film are diffusely reflected. FIG. 1A, shows how incident light can be diffusely reflected off a surface and scattered in many directions. Diffuse reflection can be caused by incident light reflecting off multi-faceted surfaces at a top surface or within an object. For example, facets of ice crystals that form a snowflake diffusely reflect incident light, rendering the snowflake white in appearance. This is in contrast to specular reflection (
The amount of perceived whiteness of a metal oxide film can be measured using any of a number of color analysis techniques. For example a color opponent process scheme, such as an L,a,b (Lab) color space based in CIE color perception schemes, can be used to determine the perceived whiteness of different oxide film samples. The Lab color scheme can predict which spectral power distributions (power per unit area per wavelength) will be perceived as the same color. In a Lab color space model, L indicates the amount of lightness, and a and b indicate color-opponent dimensions. In some embodiments described herein, the white metal oxide films have L values ranging from about 85 to 100 and a,b values of nearly zero. Therefore, these metal oxide films are bright and color-neutral.
Some embodiments described herein involve forming crystalline portions of metal oxide within an oxide film such that incident light diffusely reflects off interfaces created by the crystalline portions, thereby imparting a white appearance to the oxide film. To illustrate,
As shown in
Crystalline portion 220 and cracks 206 can have any suitable shape and size. As described above, crystalline portion 220 can include a portion or make up substantially the entire metal oxide material of oxide layer 204. If substantially the entire metal oxide material of oxide layer 204 is in a crystalline form, cracks 206 can be formed throughout oxide layer 204. Note that the size of cracks 206 are generally smaller than as depicted in
Crystalline portion 220 or cracks 206 can be formed using any suitable procedure. In some embodiments, crystalline portion 220 or cracks 206 are formed using a laser procedure. In some embodiments, crystalline portion 220 and cracks 206 are formed using other heating processes such as a plasma process. In some embodiments, the laser is tuned to form crystalline portion 220 or cracks 206 within oxide layer 204 between the top surface 214 of substrate 202 and top surface 208 of oxide layer 204. This can be accomplished by directing a laser beam at oxide layer 204 such that energy from the laser beam is focused on local areas within oxide layer 204. The energy causes the metal oxide material in the local areas to melt. As the melted oxide material cools, it can re-solidify in a crystalline form. In some embodiments, the cooling process can form cracks 206. To illustrate,
At 3A, laser beam 310 is directed at top surface 308 of oxide layer 304. Laser beam 310 is tuned to generate enough heat to melt localized portions of the metal oxide material of oxide layer 304. In some embodiments, laser beam 310 is scanned over substantially the entire top surface 308 of oxide layer 304 to melt substantially all of oxide layer 304. Laser beam 310 parameters such as wavelength, spatial energy distribution (e.g., spot size and beam shape), and temporal energy distribution (e.g., pulse duration and pulse separation) can be adjusted to cause a sufficient amount of energy to heat and melt the metal oxide but not so high an energy to negatively impact the structural integrity of oxide layer 304 too much. In some embodiments, the metal oxide material within oxide layer 304 is heated to a temperature of about 600 degrees C. or greater. In some embodiments, the metal oxide material within oxide layer 304 is heated to a temperature ranging between about 600 and 1200 degrees C. In some embodiments, the wavelength of laser beam 310 ranges within the infrared spectrum of light. In some embodiments, a CO2 laser is used, which produces infrared laser light having principle wavelength bands centering around 9.4 and 10.6 micrometers.
Laser beam 310 is tuned such that depth of focus (DOF) 318 is positioned within oxide layer 304 between top surface 308 of oxide layer 304 and top surface 314 of substrate 302. In some embodiments, spot size of laser beam 310 is small enough to melt localized portions within oxide layer 304 without substantially affecting surrounding portions of metal oxide material. In general, a smaller spot size corresponds to a smaller beam waist 317, a larger beam width 316, a smaller DOF 318, and a higher energy density (e.g., Joules/cm2). In some embodiments, the spot size and DOF 318 are each less than about 10 micrometers. In some embodiments, the spot size and DOF 318 each range from about one micrometer and about 10 micrometers. It should be noted that the spot size and DOF 318 used in the applications described herein for melting localized portions within a metal oxide film are generally small compared to traditional laser ablating and marking procedures. For example, typical laser marking applications use a spot size in the range of about 20 micrometers and 100 micrometers and a DOF 318 in the range of about 100 micrometers to about 200 micrometers. In addition, the beam width 316 used in the applications described herein are generally large compared to traditional laser ablating and marking procedures. In some embodiments, the shape of laser beam 310 is adjusted to optimize the effect of laser beam 310 on oxide layer 304. For example, a Gaussian beam shape (as shown in
As described above, in some embodiments, oxide layer 304 can be formed using any suitable method. In some embodiments, methods such as plasma electrolytic oxidation are used to form oxide layer 304 that is in largely crystalline form. In some embodiments, an anodizing process is used to form oxide layer 304 that is in largely amorphous form. In some embodiments, the laser is tuned to reflect off of the top surface of an underlying substrate and back onto the oxide layer to cause melting within the oxide layer. To illustrate,
In some embodiments, the laser beam is directed at an oxide layer at a non-normal angle relative to a top surface of the oxide layer.
An amount of whiteness of an oxide film can be adjusted by choosing an amount of spots of crystalline metal oxide material or cracks within the oxide film, the spatial distances between the spots within the oxide film, and the depth of the spots within the oxide film. The spots can be formed in patterns within an oxide films. In some embodiments, the spots are formed in clusters within spots as described above with reference to
The crystalline metal oxide portions or cracks can be positioned at any suitable depth within an oxide layer. To illustrate,
At 804, the at least one melted portion of the oxide layer is allowed to cool, thereby forming light diffusing surfaces within the oxide layer. In some embodiments, the cooling process causes the metal oxide material to re-solidify in crystalline form. In some embodiments, the cooling process causes the metal oxide material to crack. In some embodiments, the cooling process forms both crystalline metal oxide and forms cracks. The crystalline metal oxide and/or cracks have surfaces that can cause light incident on the top surface of the oxide layer to diffusely reflect, imparting a white appearance to the oxide layer. In some embodiments, the crystalline metal oxide or cracks are formed beneath the top surface of the oxide layer, thereby leaving a continuous, un-affected and un-cracked top surface. The crystalline metal oxide portions or cracks can be formed in any suitable pattern within the oxide layer and at any suitable depth within the oxide layer. In some embodiments, the depth and pattern of crystalline metal oxide portions or cracks is chosen to achieve a predetermined whiteness of the oxide layer.
As described above, specular reflection involves reflection of light in one direction. Objects that specularly reflect light will have a mirror-like quality. In contrast, diffuse reflection involves scattering of light resulting in objects appearing white. In some applications, it can be desirable for an oxide film to both diffusely and specularly reflect visible light, resulting in a white and bright appearance. The relative amount of diffuse reflection and specular reflection can be adjusted to accomplish a particular white and bright appearance. To illustrate,
Second portion 912 does not substantially include any spots of crystalline metal oxide or cracks and is substantially translucent or transparent. As such, at least some light incident top surface 908 can travel through second portion 912 and reflect off top surface 922 of substrate 902. If top surface 922 is a specularly reflective surface, such as a polished shiny metal surface, light will reflect off of top surface 922. For instance, light ray 918 entering top surface 908 travels through oxide layer 904, reflects off top surface 922, and exits top surface 908 at a first angle. Light ray 920 entering top surface 908 travels through oxide layer 904, reflects off top surface 922, and exits top surface 908 also at the first angle. In this way, the specularly reflective top surface 922 of substrate 902 can be visible through second portion 912 of oxide layer 904 and impart a shiny mirror-like shine to the portion of part 900 corresponding to second portion 912. This combination of diffuse and specular reflection gives part 900 a white and bright appearance. The relative amount of diffuse and specular reflection can be adjusted by choosing an amount of portions of oxide layer 904 having spots 906. The amount of specular reflection of part 900 can be measured using any of a number of light reflection measurement techniques. In some embodiments, a spectrometer configured to measure specular light intensity at specified angles can be used. The measure of specular light intensity is associated with an amount of lightness and L value, as described above. In some embodiments, the amount of specular reflection is compared against a standard to achieve a predetermined amount of specular reflection for part 900.
At 958, it is determined from the comparison whether the amount of specular reflectance of the white oxide film is too high. If the specular reflectance is too high, at 960, a new cracking process is designed that has an increased amount of diffuse reflectance. The amount of diffuse reflectance can be increased by increasing the amount of crystalline metal oxide portions or cracks within the oxide film, or changing the positions of the crystalline metal oxide portions or cracks within the oxide film, such as described above with reference to
In some embodiments, the underlying substrate surface has a different surface quality than a specularly reflective shine. For example, the underlying substrate can have a roughened surface that absorbs incident light and therefore has a dark or black appearance.
In some embodiments, the cracks are formed in a pattern such that a portion of the part appears white while other portions of the part appear as a different color.
In some embodiments, second portion 1103 is substantially translucent or transparent, thereby allowing the underlying metal substrate to show. In some embodiments, the underlying substrate is an aluminum or aluminum alloy and has a silver or grey color that can at least be partially visible through second portion 1103. In some embodiments, the underlying substrate has a reflective surface (e.g., mirror-like shine) that is at least partially visible through second portion 1103, as described above. In some embodiments, second portion 1103 has one or more coloring agents to impart a color to second portion 1103. For example, second portion 1103 can include one or more dye, metal, or metal oxide agents infused within the pores of the oxide material of second portion 1103. In some embodiments, first portion 1102 includes one or more coloring agents that can enhance its white color. For example, first portion 1102 can have one or more dye, metal, and metal oxide agents infused within the pores of the oxide material of first portion 1102.
In some embodiments, the cracks are formed subsequent to an oxide film dyeing process such that forming the cracks modifies the color of the dye and results in an oxide film having a different color than imparted by the dye itself. To illustrate,
At 1304, an optical quality of the oxide layer is measured after the melting treatment. A color of the treated oxide layer can be measured using any suitable colorimetric methods including, but not limited to, use of a colorimeter, spectrometer and/or a spectrophotometer. The brightness can be measured using any suitable method including, but not limited to, photometric techniques and/or radiometric techniques. At 1306, the optical quality measurement of the treated oxide layer is compared to a target optical quality measurement. In some embodiments, the target optical quality is obtained by measuring the optical quality measurements of a sample that has a predetermined desired optical quality, such as a predefined color or brightness measurement. At 1308, it is determined whether the measured optical quality of the treated oxide layer has achieved the target optical quality. If the target optical quality has not been achieved, at 1310, a new process is design wherein the amount or position of the light diffusing within an oxide layer is adjusted. Then, at 1302, another oxide layer is formed using the new process. This process is repeated until at 1308, the target optical quality is achieved and the process of flowchart 1300 is complete.
The foregoing description, for purposes of explanation, used specific nomenclature to provide a thorough understanding of the described embodiments. However, it will be apparent to one skilled in the art that the specific details are not required in order to practice the described embodiments. Thus, the foregoing descriptions of the specific embodiments described herein are presented for purposes of illustration and description. They are not target to be exhaustive or to limit the embodiments to the precise forms disclosed. It will be apparent to one of ordinary skill in the art that many modifications and variations are possible in view of the above teachings.
This Application is a continuation of U.S. application Ser. No. 14/261,060, filed Apr. 24, 2014, entitled “FORMING WHITE METAL OXIDE FILMS BY OXIDE STRUCTURE MODIFICATION OR SUBSURFACE CRACKING,” issued Dec. 12, 2017 as U.S. Pat. No. 9,839,974, which claims the benefit of U.S. Provisional Application No. 61/903,890 filed Nov. 13, 2013, entitled “FORMING WHITE METAL OXIDE FILMS BY OXIDE STRUCTURE MODIFICATION OR SUBSURFACE CRACKING,” the contents of which are incorporated by reference herein in their entirety for all purposes.
Number | Name | Date | Kind |
---|---|---|---|
3747117 | Fechter | Jul 1973 | A |
3765994 | Quaintance et al. | Oct 1973 | A |
4210499 | Hirono et al. | Jul 1980 | A |
4519876 | Lee et al. | May 1985 | A |
4753863 | Spanjer | Jun 1988 | A |
4972061 | Duley et al. | Nov 1990 | A |
5472788 | Benitez-Garriga | Dec 1995 | A |
5510015 | Martinez et al. | Apr 1996 | A |
6083871 | Fromson et al. | Jul 2000 | A |
6127050 | Fromson et al. | Oct 2000 | A |
6139713 | Masuda et al. | Oct 2000 | A |
6180415 | Schultz et al. | Jan 2001 | B1 |
6238847 | Axtell et al. | May 2001 | B1 |
6271162 | Haug et al. | Aug 2001 | B1 |
6548264 | Tan et al. | Apr 2003 | B1 |
6613161 | Zheng et al. | Sep 2003 | B2 |
6777098 | Yeo | Aug 2004 | B2 |
6821305 | Yan | Nov 2004 | B2 |
6866710 | Heider et al. | Mar 2005 | B2 |
6884336 | Kia et al. | Apr 2005 | B2 |
7144627 | Halas et al. | Dec 2006 | B2 |
7173276 | Choi et al. | Feb 2007 | B2 |
7187396 | Carroll, Jr. et al. | Mar 2007 | B2 |
7314649 | Karunaratne et al. | Jan 2008 | B2 |
8029554 | Holman et al. | Oct 2011 | B2 |
8993921 | Browning et al. | Mar 2015 | B2 |
9181629 | Browning et al. | Nov 2015 | B2 |
9403293 | Isurugi et al. | Aug 2016 | B2 |
9493876 | Browning et al. | Nov 2016 | B2 |
9839974 | McDonald et al. | Dec 2017 | B2 |
20020132105 | Robertson et al. | Sep 2002 | A1 |
20020171732 | Carroll, Jr. et al. | Nov 2002 | A1 |
20030001150 | Iwasaki et al. | Jan 2003 | A1 |
20030176563 | Kuroda et al. | Sep 2003 | A1 |
20040194235 | Yan | Oct 2004 | A1 |
20050069683 | Aylward et al. | Mar 2005 | A1 |
20050175836 | Kuehnle et al. | Aug 2005 | A1 |
20050211566 | Tomita et al. | Sep 2005 | A1 |
20060066579 | Bladt | Mar 2006 | A1 |
20060197953 | Perez et al. | Sep 2006 | A1 |
20060254922 | Brevnov et al. | Nov 2006 | A1 |
20060260947 | Kia et al. | Nov 2006 | A1 |
20070141342 | Kuehnle et al. | Jun 2007 | A1 |
20070190298 | Hampden-Smith et al. | Aug 2007 | A1 |
20070281140 | Haubrich et al. | Dec 2007 | A1 |
20070284261 | Shimotani et al. | Dec 2007 | A1 |
20080026207 | Fink-Petri et al. | Jan 2008 | A1 |
20080057293 | Hatanaka et al. | Mar 2008 | A1 |
20080073220 | Doyle | Mar 2008 | A1 |
20080274375 | Ng et al. | Nov 2008 | A1 |
20090022995 | Graham et al. | Jan 2009 | A1 |
20090120358 | Harada et al. | May 2009 | A1 |
20090130436 | Harada et al. | May 2009 | A1 |
20090181262 | Isaksson et al. | Jul 2009 | A1 |
20090323171 | Gibson | Dec 2009 | A1 |
20100015558 | Jarvis et al. | Jan 2010 | A1 |
20100183869 | Lin et al. | Jul 2010 | A1 |
20100187119 | Almond et al. | Jul 2010 | A1 |
20100215926 | Askin et al. | Aug 2010 | A1 |
20100224026 | Brennan Fournet et al. | Sep 2010 | A1 |
20110008602 | Peeters | Jan 2011 | A1 |
20110123737 | Nashner | May 2011 | A1 |
20110193928 | Zhang | Aug 2011 | A1 |
20110284381 | Cabot et al. | Nov 2011 | A1 |
20120021120 | Feldstein | Jan 2012 | A1 |
20120091495 | Hatanaka et al. | Apr 2012 | A1 |
20130224406 | Chang et al. | Aug 2013 | A1 |
20140076600 | Browning et al. | Mar 2014 | A1 |
20140209467 | Miao et al. | Jul 2014 | A1 |
20150090598 | Tatebe et al. | Apr 2015 | A1 |
20150176146 | Browning et al. | Jun 2015 | A1 |
20150225867 | Tatebe et al. | Aug 2015 | A1 |
20160024680 | Browning et al. | Jan 2016 | A1 |
20190106803 | Browning et al. | Apr 2019 | A1 |
Number | Date | Country |
---|---|---|
85103365 | Dec 1986 | CN |
1336878 | Feb 2002 | CN |
1596290 | Mar 2005 | CN |
101230474 | Jul 2008 | CN |
101275264 | Oct 2008 | CN |
102162115 | Aug 2011 | CN |
102460749 | May 2012 | CN |
102498240 | Jun 2012 | CN |
102834551 | Dec 2012 | CN |
103014706 | Apr 2013 | CN |
10134559 | Feb 2003 | DE |
993964 | Apr 2000 | EP |
1110660 | Jun 2001 | EP |
1110660 | Mar 2002 | EP |
1967616 | Sep 2008 | EP |
2649224 | Oct 2013 | EP |
60197897 | Oct 1985 | JP |
S60197897 | Oct 1985 | JP |
S62020898 | Jan 1987 | JP |
S63179098 | Jul 1988 | JP |
S63206499 | Aug 1988 | JP |
01205094 | Aug 1989 | JP |
H01205094 | Aug 1989 | JP |
H06317921 | Nov 1994 | JP |
H10121292 | May 1998 | JP |
2009221140 | Oct 2009 | JP |
2010072616 | Apr 2010 | JP |
2013084954 | May 2013 | JP |
20080031966 | Apr 2008 | KR |
20080098331 | Nov 2008 | KR |
200524460 | Jul 2005 | TW |
200714747 | Apr 2007 | TW |
2011077899 | Jun 2011 | WO |
2012076467 | Jun 2012 | WO |
2014130451 | Aug 2014 | WO |
2014130452 | Aug 2014 | WO |
2014130453 | Aug 2014 | WO |
Entry |
---|
Furneaux et al.; “The formation of controlled-porosity membranes from anodically oxidized Aluminium”, Nature, vol. 337, Jan. 1989, pp. 147-149. |
Masuda; “Highly ordered metal nanohole arrays based on anodized alumina”, Solid State Physics, vol. 31, No. 5, Dec. 1996, pp. 493-499. |
International Search Report and Written Opinion for Application No. PCT/US2013/047163 dated Sep. 25, 2013. |
Taiwanese Patent Application No. 104120036—Office Action dated Feb. 15, 2016. |
Korean Patent Application No. 10-2015-7001318—Notice of Preliminary Rejection dated Feb. 28, 2016. |
Japanese Patent Application No. 2015-518627—First Office Action dated Feb. 29, 2016. |
Chinese Application for Invention No. 201380032781.6—First Office Action dated Apr. 27, 2016. |
Hashimoto et al., “Ag Nanoparticle Films for Color Applications”, Sep. 2011, , Sep. 2011, Mater. Res. Symp. Proc., vol. 1343, pp. 1-6. |
International Search Report and Written Opinion for Application No. PCT/US2013/059793 dated Dec. 23, 2013. |
Wang et al., “Tuning color by pore depth of metal-coated porous alumina-—” Nanotechnology, vol. 22, No. 30, Art. No. 305306, pp. 1-6 (2011). |
Huang et al., “Optical characteristics of pore size on porous anodic aluminum oxide films with embedded silver nanoparticles.” Sensors & Actuators A: Physical, vol. 180, pp. 49-54. (Apr. 7, 2012). |
Hu et al., “Photosensitive gold-nanoparticle-embedded dielectric nanowires—” Nature Materials vol. 5, No. 2, pp. 102-106 (2006). |
Li et al., “Brilliant and tunable color by changing pore diameter of metal-coated porous anodic alumina.” SPIE Proceedings, vol. 8564, pp. 85640-1-85640-6 (Nov. 20, 2012). |
International Search Report and Written Opinion for Application No. PCT/US14/051527 dated Nov. 24, 2014. |
Sunada et al.; “Dielectric properties of Al—Si composite oxide films formed on electropolished and DC-etched aluminum by electrophoretic sol-gel coating and anodizing.” J. Solid State Electrochem. vol. 11, No. 10:1375-1384 (Oct. 2007). |
Chen et al., “The effect of anodizing voltage on the electrical properties of A1-Ti composite oxide film on aluminum.” J. Electroanalytic Chem. vol. 590, No. 1:26-31 (May 2006). |
Korean Patent Application No. 2015-7001318—First Office Action dated Sep. 26, 2016. |
Regone et. al.; J. Mat. Process. Tech., 172 (2006), 146-151. |
Curran et al.; Surface and Coatings Technology, 199 (2005), 168-176. |
AlMawlawi, et. al. “Magnetic properties of Fe deposited into anodic aluminum oxide pores as a function of particle size”, AIP Journal of Applied Physics, vol. 70, No. 8, Oct. 15, 1991, 4421-4425. |
Chen et al.; “Synthesis of anodizing composite films containing superfine Ah03 and PTFE particles on Al alloys”, Applied Surface Science. 256, Apr. 20, 2010, pp. 6418-6525. |
Chinese Application Patent No. 201480059602.2—Office Action dated Mar. 24, 2017. |
European Patent Application No. 14857882.6—Extended European Search Report dated Jun. 21, 2017. |
Vreeling et al., “Laser melt injection in aluminum alloys: on the role of the oxide skin”, Acta Materialia., vol. 48, No. 17, Nov. 2000 (Nov. 2000), pp. 4225-4233, 9 pages. |
Korean Patent Application No. 10-2017-7017085—Office Action dated Jul. 20, 2017. |
Japanese Patent Application No. 2016-153985—Office Action dated Sep. 29, 2017. |
Chinese Application Patent No. 201480059602.2—Second Office Action dated Sep. 27, 2017. |
Japanese Patent Application No. 2016-153985—Final Rejection dated Apr. 20, 2018. |
Ohinese Application for Invention No. 201711079453.8—First Office Action dated Dec. 28, 2018. |
Chinese Application Patent No. 201480059602.2—Rejection Decision dated Dec. 28, 2018. |
Number | Date | Country | |
---|---|---|---|
20180099352 A1 | Apr 2018 | US |
Number | Date | Country | |
---|---|---|---|
61903890 | Nov 2013 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 14261060 | Apr 2014 | US |
Child | 15817010 | US |