Classifications

• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
  • C03C17/28—Surface treatment of glass, not in the form of fibres or filaments, by coating with organic material
  • C03C17/30—Surface treatment of glass, not in the form of fibres or filaments, by coating with organic material with silicon-containing compounds
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
  • C03C17/34—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
  • C03C17/42—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating of an organic material and at least one non-metal coating
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C21/00—Treatment of glass, not in the form of fibres or filaments, by diffusing ions or metals in the surface
  • C03C21/001—Treatment of glass, not in the form of fibres or filaments, by diffusing ions or metals in the surface in liquid phase, e.g. molten salts, solutions
  • C03C21/002—Treatment of glass, not in the form of fibres or filaments, by diffusing ions or metals in the surface in liquid phase, e.g. molten salts, solutions to perform ion-exchange between alkali ions
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C3/00—Glass compositions
  • C03C3/04—Glass compositions containing silica
  • C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
  • C03C3/083—Glass compositions containing silica with 40% to 90% silica, by weight containing aluminium oxide or an iron compound
  • C03C3/085—Glass compositions containing silica with 40% to 90% silica, by weight containing aluminium oxide or an iron compound containing an oxide of a divalent metal
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C3/00—Glass compositions
  • C03C3/04—Glass compositions containing silica
  • C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
  • C03C3/083—Glass compositions containing silica with 40% to 90% silica, by weight containing aluminium oxide or an iron compound
  • C03C3/085—Glass compositions containing silica with 40% to 90% silica, by weight containing aluminium oxide or an iron compound containing an oxide of a divalent metal
  • C03C3/087—Glass compositions containing silica with 40% to 90% silica, by weight containing aluminium oxide or an iron compound containing an oxide of a divalent metal containing calcium oxide, e.g. common sheet or container glass
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C3/00—Glass compositions
  • C03C3/04—Glass compositions containing silica
  • C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
  • C03C3/089—Glass compositions containing silica with 40% to 90% silica, by weight containing boron
  • C03C3/091—Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C2217/00—Coatings on glass
  • C03C2217/40—Coatings comprising at least one inhomogeneous layer
  • C03C2217/42—Coatings comprising at least one inhomogeneous layer consisting of particles only
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C2217/00—Coatings on glass
  • C03C2217/70—Properties of coatings
  • C03C2217/73—Anti-reflective coatings with specific characteristics
  • C03C2217/732—Anti-reflective coatings with specific characteristics made of a single layer
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C2217/00—Coatings on glass
  • C03C2217/70—Properties of coatings
  • C03C2217/75—Hydrophilic and oleophilic coatings
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C2217/00—Coatings on glass
  • C03C2217/70—Properties of coatings
  • C03C2217/76—Hydrophobic and oleophobic coatings
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C2217/00—Coatings on glass
  • C03C2217/70—Properties of coatings
  • C03C2217/77—Coatings having a rough surface
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C2218/00—Methods for coating glass
  • C03C2218/30—Aspects of methods for coating glass not covered above
  • C03C2218/31—Pre-treatment
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
  • Y10T428/24355—Continuous and nonuniform or irregular surface on layer or component [e.g., roofing, etc.]
  • Y10T428/24364—Continuous and nonuniform or irregular surface on layer or component [e.g., roofing, etc.] with transparent or protective coating
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
  • Y10T428/24942—Structurally defined web or sheet [e.g., overall dimension, etc.] including components having same physical characteristic in differing degree
  • Y10T428/2495—Thickness [relative or absolute]
  • Y10T428/24967—Absolute thicknesses specified
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/26—Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
  • Y10T428/266—Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension of base or substrate

Definitions

• Provisional Application Serial No. 61/026289 filed on February 5, 2008 and claims the benefit of priority under 35 U.S.C. ⁇ 1 19(e) of U.S. Provisional Application Serial No. 61/130532 filed on May 30, 2008.
• the invention relates to an alkali aluminosilicate glass. More particularly, the invention relates to a high strength, down-drawn alkali aluminosilicate glass article for use a protective cover plate. Even more particularly, the invention relates to a high strength, down-drawn alkali aluminosilicate amphiphobic glass for use as a cover plate in mobile electronic devices.
• Mobile electronic devices such as personal data assistants, mobile or cellular telephones, watches, laptop computers and notebooks, and the like, often incorporate a cover plate. At least a portion of the cover plate is transparent, so as to allow the user to view a display. For some applications, the cover plate is sensitive to the user's touch. Due to frequent contact, such cover plates must have high strength and be scratch resistant.
• U.S. Patent Application No. 1 1/888213 assigned the instant assignee discloses alkali aluminosilicate glass that is capable being chemically strengthened by ion- exchange and exhibits a composition which can be down-drawn into sheets.
• the glass has a melting temperature of less than about 1650 0 C and a liquidus viscosity of at least 130 kpoise and, in one embodiment, greater than 250 kpoise.
• the glass can be ion- exchanged at relatively low temperatures and to a depth of at least 30 ⁇ m.
• the glass comprises: 64 mol% ⁇ SiO 2 ⁇ 68 mol%; 12 mol% ⁇ Na 2 O ⁇ 16 mol%; 8 mol% ⁇ Al 2 O 3 ⁇ 12 mol%; 0 mol% ⁇ B 2 O 3 ⁇ 3 mol%; 2 mol% ⁇ K 2 O ⁇ 5 mol%; 4 mol% ⁇ MgO ⁇ 6 mol%; and 0 mol% ⁇ CaO ⁇ 5 mol%, wherein: 66 mol% ⁇ SiO 2 + B 2 O 3 + CaO ⁇ 69 mol%; Na 2 O + K 2 O + B 2 O 3 + MgO + CaO + SrO > 10 mol%; 5 mol% ⁇ MgO + CaO + SrO ⁇ 8 mol%; (Na 2 O + B 2 O 3 ) - Al 2 O 3 ⁇ 2 mol%; 2 mol% ⁇ Na 2 O - Al 2 O 3 ⁇ 6 mol%; and 4
• This alkali aluminosilicate glass can be used as a damage resistant cover glass for use in electronic products.
• the glass is finished to shape and then chemically tempered, or ion-exchanged (IOXed), to form a compressive surface layer that prevents mechanical damage such as scratching and abrasion, thus imparting damage resistance.
• IOXed chemically tempered, or ion-exchanged
• the IOX process works by exchanging larger potassium ions for smaller sodium ions at the surface of the glass, with time and temperature of the process driving the depth of exchange and imparting a compressive "depth of layer” (DOL) that, if deeper than damage induced to the surface during product use, prevents breakage.
• DOL compressive "depth of layer”
• a second critical issue is glare that can arise from reflections on the display surface. Glare arises from the reflection of light that is not normal to the field of the operator's view. The presence of glare causes the use to tilt the device and continually adjust the screen angle for better viewing. Having to constantly change their angle of viewing is irksome to the user and creates dissatisfaction.
• any display surface that includes anti-reflection (“AR”) properties would make fingerprints more evident, as tilting of non-AR coated surfaces negates out fingerprints with glare.
• AR anti-reflection
• the invention in one embodiment relates to a product consisting of a transparent, damage resistant, chemically toughened protective cover glass (also called a cover plate or cover screen) that has an exterior coating having fluorine termination groups that impart a degree of hydrophobicity and oleophobicity (i.e., amphiphobicity) to the cover glass such that wetting of the glass surface by water and oils is minimized.
• a transparent, damage resistant, chemically toughened protective cover glass also called a cover plate or cover screen
• an exterior coating having fluorine termination groups that impart a degree of hydrophobicity and oleophobicity (i.e., amphiphobicity) to the cover glass such that wetting of the glass surface by water and oils is minimized.
• the coated product has scratch, abrasion, and other damage resistance imparted by the compressive surface DOL of the glass, and additionally has anti-fingerprint, anti-smudge characteristics imparted by the fluorine termination groups that minimize the transport of oils from finger to the glass (fingerprints) and further allows for ease of removal of the oils/fingerprints by means of wiping with a cloth.
• the invention relates to a product consisting of a transparent damage resistant chemically protective cover glass having at least one chemically toughened layer and a non- chemically toughened layer; said cover glass having a exterior coating of fluorine termination groups that impart a degree of hydrophobicity and oleophobicity.
• the invention relates to a product consisting of a transparent damage resistant chemically protective cover glass having a non-chemically toughened layer sandwiched between two chemically toughened layers and; said cover glass having a exterior coating of fluorine termination groups that impart a degree of hydrophobicity and oleophobicity.
• the chemical toughened layers are formed by ion exchange of Na and/or Li ions by K ions.
• the cover glass may have a non chemically toughened layer sandwiched between two chemically toughened layers in which Na and/or Li ions have been exchanged by K ions.
• the present invention provides an alkali aluminosilicate glass article having a thickness of at least approximately 0.3 mm, a surface compressive stress of at least about 200 MPa, a surface compressive layer having a depth of at between approximately 20-70 ⁇ m, and having an amphiphobic adsorbed fluorine-based surface layer.
• the adsorbed fluorine-based surface layer is formed by exchanging the hydrogen of glass terminal OH groups with a fluorine-based moiety, for example a fluorine containing monomer, to form a glass having terminal fluorinated groups.
• a fluorine-based moiety for example a fluorine containing monomer
• the exchange can be carried out according to the reaction
• Rp is a C 1 -C 22 alkyl perfluorocarbon or C 1 -C 22 alkyl perfluoropolyether, preferably C 1 -C 10 alkyl perfluorocarbon and more preferably a C 1 -C] 0 alkyl perfluoropolyether;
• n is an integer in the range of 1-3; and
• X is a hydrolyzable group that can be exchanged with the glass terminal OH groups.
• X is a halogen other than fluorine or an alkoxy group (-OR) where R is a linear or branched hydrocarbon of 1-6 carbon atom, for example without limitation, -CH 3 , -C 2 H 5 , -CH(CH 3 ) 2 hydrocarbons.
• n 2 or 3, preferably 3.
• the preferred halogen is chlorine.
• a preferred alkoxysilane is a trimethoxy silane, RpSi(OMe) 3 .
• perfluorocarbon moieties that can be used in practicing the invention include (Rp) 3 SiCl, R F - C(O)-Cl, R F - C(O)-NH 2 , and other perfluorocarbon moieties having a terminal group exchangeable with a glass hydroxyl (OH) group.
• perfluorocarbon means a compound having hydrocarbon groups as described herein in which substantially all of the C-H bonds have been converted into C-F bonds.
• the adsorbed fluorine-based surface layer is comprised of an assembled monolayer of a fluorine-terminating molecular chain.
• the adsorbed fluorine-based surface layer is comprised of a thin, fluoro- polymeric coating.
• the adsorbed fluorine-based surface layer is comprised of silica soot particles having pendent fluorocarbon groups attached to the soot particles.
• the invention in a further embodiment, relates to a product consisting of a transparent, damage resistant, chemically toughened protective cover glass that has an anti-reflective layer, for example without limitation, an anti-reflective SiO 2 or F-SiO 2 (fluorine doped silica or fused silica) layer, and further has an exterior coating having fluorine termination groups that impart a degree of hydrophobicity and oleophobicity (i.e., amphiphobicity) to the cover glass such that wetting of the glass surface by water and oils is minimized.
• Abrasion resistance is imparted to the anti-reflective article by applying a final coating of an amphiphobic material as described herein.
• the amphiphobic material coated product has scratch, abrasion, and otherwise damage resistance imparted by the compressive surface DOL of the glass, and additionally has anti-fingerprint, anti-smudge characteristics imparted by the fluorine termination groups that minimizes the transport of oils and sweat from finger to the glass (fingerprints) and further allows for ease of removal of the oils/fingerprints by means of wiping with a cloth.
• the AR coating can have a lower abrasion/scratch resistance than the underlying chemically strengthened base glass.
• the exterior (outermost) layer of the AR coating is a SiO 2 -containing layer; for example F-SiO 2 , fused silica or silica.
• the alkali aluminosilicate glass article may further include a textured or patterned surface located between base glass and the fluorine-based surface coating layer.
• Texture can be derived by acid/alkali etch including combinations thereof, to produce a roughness in the range of 50 run to 5 ⁇ M (5000 nm) in RMS roughness, the composition of the roughened glass at near-surface preferably being rich in SiO 2 .
• the roughness can be measured by techniques such as Atomic Force Microscopy ("AFM") and Scanning White Light Interferometry (SWLI).
• the texture can be derived lithographically or using otherwise deposited structures, again with the composition of the roughened glass at near-surface preferably being rich in SiO 2 .
• the textured layer and any untextured base glass is then coated with a fluorine-containing materials as described herein to form an article having a textured, fluorine-containing material coated article.
• Figure 1 is a schematic of the alkali aluminosilicate glass article according to one embodiment and illustrates an article in which a layer of an amphiphobic perfluorocarbon or perfluorocarbon containing moiety is covalently bonded to the surface of a chemically strengthened glass.
• Figure 2 is a schematic of a chemically strengthened alkali aluminosilicate glass article according to a second embodiment and illustrates an article in which a textured or patterned surface is present and an amphiphobic layer is covalently bonded to the surface of a chemically strengthened glass including the textured area.
• Figure 3 is a schematic of an alkali aluminosilicate glass according to an additional embodiment of the invention and illustrates an article in which at least one layer of an anti-reflective material is placed on top a chemically strengthened glass layer and an amphiphobic coating layer is covalently bonded to the surface of the anti-reflective coating.
• Figure 4 is a schematic illustrating the generic process flow for preparing glass surfaces for coating with an amphiphobic coating.
• Figure 5A illustrates wiping performance to reduce haze and thus improve optical clarity of coated glass versus non-coated glass.
• Figure 5B shows the cover glass represented in Figure 5A, left side uncoated and right side coated, after fingerprint oil has been applied and wiped.
• Figure 5C shows a cover glass, left side uncoated and right side coated, after abrasion with 150 grit sandpaper and wiping.
• Figure 6 illustrates the haze generated by abrasion with 150 grit sandpaper using coated glass and non-coated glass.
• Figure 7 illustrates the kinetic effect of friction, ⁇ 5 of coated and non-coated glass surfaces.
• Figure 8 is a bar chart showing wiping results for a glass sample one-half treated with acid and one-half not acid treated, both halves being coated with an amphiphobic coating.
• base glass refers to any alkali aluminoborosilicate glass suitable for forming a protective cover glass before such glass undergoes ion-exchange or coating with any material, for example, an antireflective coating and/or a perfluorocarbon material or moiety to impart oil and smudge resistance.
• SiO 2 coating means either a SiO 2 coating or F-SiO 2 coating, or a composite SiO 2 /F-SiO 2 coating.
• the perfluorocarbon moiety or perfluorocarbon-containing moiety (as a layer or coating) is bonded to the surface of the glass, the chemically strengthened glass, or the chemically strengthened and SiO 2 (or F-SiO 2 ) coated glass by covalent bonds.
• the term "amphiphobic" is used to denote a material that when applied to a surface imparts both hydrophobic and oleophobic properties to the surface.
• a transparent, protective cover glass article that has enhanced damage resistance and amphiphobic properties, thus providing a scratch resistance surface that exhibits minimal fingerprint adherence and ease of fingerprint removal.
• Figure 1 specifically illustrates alkali aluminosilicate glass article 100 having a thickness of at least 0.3 mm, a surface compressive stress layers 104 having a surface compressive stress of at least 200 MPa and middle glass layer 106.
• the surface compressive layer 104 has a thickness in the range of 20-70 ⁇ m; typically achieved through an ion-exchange process as described below.
• the article 100 has an amphiphobic adsorbed fluorine-based surface layer 102.
• the adsorbed fluorine-based surface layer or coating can be achieved in any number of ways and can be selected from the group consisting of: (1) -OH group terminated active surface sites exchanged with a fluorine-based monomer; (2) an assembled monolayer of a fluorine-terminating molecular chain; (3) a thin, fluoro- polymeric coating; (4) silica soot particles which have been previous derived with or treated to have fluorine termination groups.
• the coating can be applied to the surface by dipping, vapor coating, spraying, application with a roller, or other suitable method. Dipping or spraying is preferred.
• the coating After the coating has been applied it is "cured" at a temperature in the range of 25-150 °C, preferably 40-100 °C, a time in the range of 1-4 hours, in an atmosphere containing 40-95% moisture.
• the coating applied to the sample shown in the Figures and discussed herein was "50/50 cured,” meaning it was cured at 50 °C in an atmosphere containing 50% moisture for 2 hours. After curing the samples were solvent rinsed to remove any unbound coating and air-dried prior to use.
• the glass article 100 includes all of the features of the Figure 1 embodiment; including the surface compressive stress layer 104, the non ion-exchanged middle layer glass portion 106 and an amphiphobic adsorbed fluorine-based surface layer 102.
• this embodiment includes a textured or patterned surface 108 located between the adsorbed fluorine-based surface layer 102 (represented by the heavy black scribble line) and the glass surface compressive layer 104.
• the textured or patterned layer is formed from the compressive layer by etching or lithography.
• the textured or patterned layer is formed by particle coatings bonded to the compressive layer 104.
• the fluorine-based layer covers both the textured/patterned layer 104 and any compressive layer that has not been textured or patterned.
• the textured or patterned surface illustrated in Figure 2 is added to the base glass or is formed on the base glass.
• the application of this textured or patterned surface can be achieved in any number of ways known to those skilled in the art. Included among the options for adding the textured/patterned surface to the base glass or forming the textured/patterned surface on the base glass are etching, electrospinning of polymer or inorganic materials, a deposited inorganic film, ordered particle coatings, or any other means for patterning or texturing a glass surface known in the art.
• the inclusion of textured or patterned surface results in a glass article that exhibits increased surface area while maintaining the required degree of transparency.
• the textured surface is coated with an amphiphobic coating as described herein.
• the amphiphobic glass articles disclosed herein exhibit the following enhanced features over commercially available protective cover glass solutions.
• the exemplary coating material used to prepare and test the samples described herein and in the Figures was DC 2604 (Dow Corning Corp, Midland, MI), an alkoxysilyl perfluoropolyether material.
• the test glass was Corning 1317 glass (Corning Incorporated, Corning NY) which was chemically strengthened as described herein; and the test glass pieces had dimensions of approximately 2 cm x 12 cm x 0.4 cm.
• the fluorine treated (and thus fluorine terminated) surface is less polar than a surface with -OH termination groups, and thus promotes minimal hydrogen (i.e., Van der Waals) bonding between particles and liquids.
• minimal hydrogen i.e., Van der Waals
• Scratch resistance testing was conducted using a glass article in which one-half of the article's face was amphiphobically coated and the other half was uncoated.
• the test was a sandpaper scratch test in which the sandpaper (150 grit) was passed across both surfaces using a reciprocating wear instrument such that both sides, coated and uncoated, were subject to equal abrasion.
• Haze was measured on both areas on both sides of the article, where haze is a measure of optical clarity in terms scattered light versus the sum of all scattered and transmitted light.
• liquidus viscosity refers to the viscosity of a molten glass at the liquidus temperature, wherein the liquidus temperature refers to the temperature at which crystals first appear as a molten glass cools down from the melting temperature, or the temperature at which the very last crystals melt away as temperature is increased from room temperature.
• the glass comprises the following oxides, the concentrations of which are expressed in mole percent (mol%): 64 ⁇ SiO 2 ⁇ 68; 12 ⁇ Na 2 O ⁇ 16; 8 ⁇ Al 2 O 3 ⁇ 12; 0 ⁇ B 2 O 3 ⁇ 3; 2 ⁇ K 2 O ⁇ 5; 4 ⁇ MgO ⁇ 6; and O ⁇ CaO ⁇ 5.
• the largest single constituent of the alkali aluminosilicate glass is SiO 2 , which forms the matrix of the glass and is present in the inventive glasses in a concentration ranging from about 64 mol% up to and including about 68 mol%.
• SiO 2 serves as a viscosity enhancer that aids formability and imparts chemical durability to the glass. At concentrations that are higher than the range given above, SiO 2 raises the melting temperature prohibitively, whereas glass durability suffers at concentrations below the range. In addition, lower SiO 2 concentrations can cause the liquidus temperature to increase substantially in glasses having high K 2 O or high MgO concentrations.
• the glasses of the present invention When present in a concentration ranging from about 8 mol% up to and including about 12 mol%, Al 2 O 3 enhances viscosity. At Al 2 O 3 concentrations that are higher than this range, the viscosity can become prohibitively high, and the liquidus temperature may become too high to sustain a continuous down-draw process. To guard against this, the glasses of the present invention have a total concentration of alkali metal oxides (e.g., Na 2 O, K 2 O) that is well in excess of the total Al 2 O 3 content.
• alkali metal oxides e.g., Na 2 O, K 2 O
• Fluxes are used to obtain melting temperatures that are suitable for a continuous manufacturing process.
• the oxides Na 2 O, K 2 O, B 2 O 3 , MgO, CaO, and SrO serve as fluxes.
• the temperature of the glass at a viscosity of 200 poise is not greater than 165O 0 C.
• Na 2 O + K 2 O + B 2 O 3 + MgO + CaO + SrO - Al 2 O 3 > 10 mol% should be met.
• Alkali metal oxides serve as aids in achieving low liquidus temperatures, and low melting temperatures.
• melting temperature refers to the temperature corresponding to a glass viscosity of 200 poise.
• Na 2 O is used to enable successful ion-exchange.
• Na 2 O is provided in a concentration ranging from about 12 mol% up to and including about 16 mol%. If, however, the glass were to consist exclusively OfNa 2 O, Al 2 O 3 , and SiO 2 within the respective ranges described herein, the viscosity would be too high to be suitable for melting. Thus, other components must be present to ensure good melting and forming performance.
• K 2 O Potassium oxide
• Na 2 O + K 2 O sodium sulfate
• Al 2 O 3 the total difference between the sum of the Na 2 O and K 2 O concentrations and the Al 2 O 3 concentration should be in a range from about 4 mol% up to and including about 10 mol% (i.e., 4 mol% ⁇ (Na 2 O + K 2 O) - Al 2 O 3 ⁇ 10 mol%).
• B 2 O 3 serves as a flux; i.e., a component added to reduce melting temperatures.
• the addition of even small amounts (i.e., less than about 1.5 mol%) OfB 2 O 3 can radically reduce melting temperatures of otherwise equivalent glasses by as much as 100 0 C.
• sodium is added to enable successful ion- exchange, it may be desirable, at relative low Na 2 O contents and high Al 2 O 3 contents, to add B 2 O 3 to ensure the formation of a meltable glass.
• the total concentration OfNa 2 O and B 2 O 3 is linked such that (Na 2 O + B 2 O 3 ) - Al 2 O 3 ⁇ 2 mol%.
• the combined concentration of SiO 2 , B 2 O 3 , and CaO ranges from about 66 mol% up to and including about 69 mol% (i.e., 66 mol% ⁇ SiO 2 + B 2 O 3 + CaO ⁇ 69 mol%).
• any alkaline earth oxides present in the glass serve primarily as fluxes.
• MgO is the most effective flux, but is prone to form forsterite (Mg 2 SiO 4 ) at low MgO concentrations in sodium aluminosilicate glasses, thus causing the liquidus temperature of the glass to rise very steeply with MgO content.
• glasses have melting temperatures that are well within the limits required for continuous manufacturing. However, the liquidus temperature may be too high - and thus the liquidus viscosity too low - to be compatible with a down-draw process such as, for example, the fusion draw process.
• the addition of at least one OfB 2 O 3 and CaO can drastically reduce the liquidus temperature of these MgO-rich compositions. Indeed, some level of B 2 O 3 , CaO, or both may be necessary to obtain a liquidus viscosity that is compatible with the fusion process, particularly in glasses having high sodium, low K 2 O, and high Al 2 O 3 concentrations.
• Strontium oxide (SrO) is expected to have precisely the same impact on liquidus temperatures of high MgO glasses as CaO.
• the alkaline earth metal oxide concentration is thus broader than the MgO concentration itself, such that 5 mol% ⁇ MgO + CaO + SrO ⁇ 8 mol%.
• Barium is also an alkaline earth metal, and additions of small amounts of barium oxide (BaO) or substitution of barium oxide for other alkaline earths may produce lower liquidus temperatures by destabilizing alkaline-earth-rich crystalline phases.
• barium is considered to be a hazardous or toxic material. Therefore, while barium oxide may be added to the glasses described herein at a level of at least 2 mol% with no deleterious impact or even with a modest improvement to liquidus viscosity, the barium oxide content is generally kept low to minimize the environmental impact of the glass. Thus, in one embodiment, the glass is substantially free of barium.
• the glasses of the present invention tend to exhibit 200 kpoise viscosities that are relatively high, between about 1500°C and 1675 0 C. Such viscosities are typical of industrial melting processes, and in some cases melting at such temperatures may be required to obtain glass with low levels of gaseous inclusions. To aid in eliminating gaseous inclusions, it may be useful to add chemical fining agents. Such fining agents fill early-stage bubbles with gas, thus increasing their rise velocity through the melt.
• Typical fining agents include, but are not limited to: oxides of arsenic, antimony, tin and cerium; metal halides (fluorides, chlorides and bromides); metal sulfates; and the like.
• Arsenic oxides are particularly effective fining agents because they release oxygen very late in the melt stage.
• arsenic and antimony are generally regarded as hazardous materials.
• the glass is substantially free of antimony and arsenic, comprising less that about 0.05 wt% of each of the oxides of these elements. Therefore, it may be advantageous in particular applications to avoid using arsenic or antimony at all, and using instead a nontoxic component such as tin, halides, or sulfates to produce a fining effect.
• Tin (IV) oxide (SnO 2 ) and combinations of tin (IV) oxide and halides are particularly useful as fining agents in the present invention.
• the glass described herein is down-drawable; that is, the glass is capable of being formed into sheets using down-draw methods such as, but not limited to, fusion draw and slot draw methods that are known to those skilled in the glass fabrication arts. Such down-draw processes are used in the large-scale manufacture of ion-exchangeable flat glass.
• the fusion draw process uses a drawing tank that has a channel for accepting molten glass raw material.
• the channel has weirs that are open at the top along the length of the channel on both sides of the channel.
• the molten glass overflows the weirs. Due to gravity, the molten glass flows down the outside surfaces of the drawing tank. These outside surfaces extend down and inwardly so that they join at an edge below the drawing tank. The two flowing glass surfaces join at this edge to fuse and form a single flowing sheet.
• the fusion draw method offers the advantage that, since the two glass films flowing over the channel fuse together, neither outside surface of the resulting glass sheet comes in contact with any part of the apparatus. Thus, the surface properties are not affected by such contact.
• the slot draw method is distinct from the fusion draw method.
• the molten raw material glass is provided to a drawing tank.
• the bottom of the drawing tank has an open slot with a nozzle that extends the length of the slot.
• the molten glass flows through the slot/nozzle and is drawn downward as a continuous sheet therethrough and into an annealing region.
• the slot draw process provides a thinner sheet, as only a single sheet is drawn through the slot, rather than two sheets being fused together, as in the fusion down-draw process.
• the alkali aluminosilicate glass described herein has a high liquidus viscosity.
• the liquidus viscosity is at least 130 kilopoise (kpoise) and, in another embodiment, the liquidus viscosity is at least 250 kpoise.
• the alkali aluminosilicate glass described herein is substantially free of lithium.
• substantially free of lithium means that lithium is not intentionally added to the glass or glass raw materials during any of the processing steps leading to the formation of the alkali aluminosilicate glass. It is understood that an alkali aluminosilicate glass or an alkali aluminosilicate glass article that is substantially free of lithium may inadvertently contain small amounts of lithium due to contamination. The absence of lithium reduces poisoning of ion-exchange baths, and thus reduces the need to replenish the salt supply needed to chemically strengthen the glass.
• the glass is compatible with continuous unit (CU) melting technologies such as the down-draw processes described above and the materials used therein, the latter including both fused zirconia and alumina refractories and zirconia and alumina isopipes.
• CU continuous unit
• the glass is chemically strengthened by ion-exchange.
• ion-exchanged is understood to mean that the glass is strengthened by ion-exchange processes that are known to those skilled in the glass fabrication arts. Such ion-exchange processes include, but are not limited to, treating the heated alkali aluminosilicate glass with a heated solution containing ions having a larger ionic radius than ions that are present in the glass surface, thus replacing the smaller ions with the larger ions. Potassium ions, for example, could replace sodium ions in the glass.
• the down-drawn glass is chemically strengthened by placing it a molten salt bath comprising KNO 3 for a predetermined time period to achieve ion-exchange.
• the temperature of the molten salt bath is about 430 0 C and the predetermined time period is about eight hours.
• the chemical strengthening by ion-exchange can be carried out on large pieces of glass which will then be cut (sliced, sawed or otherwise processed) to the size appropriate for the specific application in which it is intended to be used or the strengthening carried out on glass pieces pre-cut to the size appropriate for the intended use.
• the down-drawn alkali aluminosilicate glass has a warpage of less than about 0.5 mm for a 300mm x 400 mm sheet. In another embodiment, the warpage is less than about 0.3 mm.
• Surface compressive stress refers to a stress caused by the substitution during chemical strengthening of an alkali metal ion contained in a glass surface layer by an alkali metal ion having a larger ionic radius.
• potassium ions are substituted for sodium ions in the surface layer of the glass described herein.
• the glass has a surface compressive stress of at least about 200 MPa. In one embodiment, the surface compressive stress is at least about 600 MPa.
• the alkali aluminosilicate glass has a compressive stress layer in parted by ion-exchange that has a depth of at least about 20 ⁇ m. In one embodiment the compressive stress layer imparted by ion-exchange is in the range of 30-80 ⁇ m.
• CS CT x (t-2DOL)/DOL, where t is the thickness of the glass and DOL is the depth of exchange.
• a lithium-free glass having a thickness of at least 0.3 mm, a surface compressive stress of at least about 200 MPa, and a surface compressive layer having a depth of at least about 30 ⁇ m is also provided.
• the compressive stress is at least about 600 MPa
• the depth of the compressive layer is at least about 40 ⁇ m
• the thickness of the lithium-free glass is in a range from about 0.7 mm up to about 1.1 mm.
• the lithium-free glass comprises: 64 mol% ⁇ SiO 2 ⁇ 68 mol%; 12 mol% ⁇ Na 2 O ⁇ 16 mol%; 8 mol% ⁇ Al 2 O 3 ⁇ 12 mol%; 0 mol% ⁇ B 2 O 3 ⁇ 3 mol%; 2 mol% ⁇ K 2 O ⁇ 5 mol%; 4 mol% ⁇ MgO ⁇ 6 mol%; and 0 mol% ⁇ CaO ⁇ 5 mol%, wherein: 66 mol% ⁇ SiO 2 + B 2 O 3 + CaO ⁇ 69 mol%; Na 2 O + K 2 O + B 2 O 3 + MgO + CaO + SrO > 10 mol%; 5 mol% ⁇ MgO + CaO + SrO ⁇ 8 mol%; (Na 2 O + B 2 O 3 ) - Al 2 O 3 ⁇ 2 mol%; 2 mol% ⁇ Na 2 O - Al 2 O 3 ⁇
• the liquidus viscosity in one embodiment is at least 250 kpoise.
• Chemically strengthened, anti-reflective, amphiphobic glass [0062]
• the invention in another embodiment, relates to a product consisting of a transparent, damage resistant, chemically strengthened protective cover glass that is coated with an antireflective SiO 2 or F-SiO 2 (silica, fused silica or fluorine-doped silica) layer and further has an exterior coating having fluorine termination groups that impart a degree of hydrophobicity and oleophobicity (i.e., amphiphobicity) to the cover glass such that wetting of the glass surface by water and oils is minimized.
• SiO 2 or F-SiO 2 silicon, fused silica or fluorine-doped silica
• the application of the amphiphobic coating to the AR-coated, chemically strengthened glass improves scratch, abrasion, and other damage resistance and further imparts anti- fingerprint, anti-smudge characteristics due to the presence of the fluorine termination groups in the amphiphobic coating that minimizes the transport of oils from finger to the glass (fingerprints) and further allows for ease of removal of the oils/fingerprints by means of wiping with cloth.
• SiO 2 coating means either a SiO 2 or F-SiO 2 coating or a composite SiO 2 /F-SiO 2 coating.
• the antireflective and abrasion resistant SiO 2 or F-SiO 2 coating can be placed on the base glass either before or after ion-exchange, preferably.
• the F-SiO 2 coating is placed on base glass that has been ion-exchanged and before the placement of any perfluorocarbon that is used to improve the removal of oils and smudges as from, for example, fingerprints.
• Perfluorocarbons are used to reduce the surface energy of glass surfaces and this is accomplished as a result of the low polarity of the fluorine terminated surface bond. It is important that the perfluorocarbon coating have sufficient durability when used by a device customer so that this protection last for a sufficient life time, typically at least two years.
• a variety of attachment chemistries can be used to attach perfluorocarbon or perfluo ' rocarbon-containing materials to a glass surface.
• glass surfaces that have been chemically strengthened by ion-exchange e.g., K ions for Na and/or Li ions in a base glass
• K ions for Na and/or Li ions in a base glass have a surface that is rich in K ions which limits the number of Si-OH active surface sites and this inhibits the covalent bonding a perfluorocarbon or perfluorocarbon-containing moiety to surface of the ion-exchanged glass.
• SiO 2 or F-SiO 2 coating One benefit of applying a SiO 2 or F-SiO 2 coating is the enhanced Si-termination sites that are present on a SiO 2 or F-SiO 2 coated chemically strengthened glass versus a chemically strengthened glass without the coating that has an alkali-rich ion-exchanged surface.
• the SiO 2 or F-SiO 2 coating over the chemically strengthened glass surface the bonding of perfluorocarbon or perfluorocarbon containing moieties is enhanced and the surface density of the covalently bonded perfluorocarbon or perfluorocarbon containing moieties is increased.
• the outermost fluorinated species generate the "Anti- Fingerprint” or "Easy-to-Clean” properties of the cover glass without loss of glass strength resulting from the chemical strengthening, hi addition, the SiO 2 or F-SiO 2 coating, by itself or in conjunction with additional layer of SiO 2 or F-SiO 2 and another metal oxide film (a multilayer coating that can have sequential layers of SiO 2 and/or F-SiO 2 and/or “other metal oxides”) can act as an anti-reflective coating.
• other metal oxides include, for example, HfO 2 , TiO 2 , ZrO 2 , Y 2 O 3 , Gd 2 O 3 , and other metal oxides known in the art to be useful for anti-reflective coatings.
• MgF 2 can be used as an anti-reflective layer and can be applied to chemically strengthened glass. The perfluorocarbon containing moieties can then be applied to the anti-reflective coating.
• the resulting coated, chemically strengthened glass has enhanced damage resistance, anti-reflection and amphiphobic properties, and thus provides a scratch resistance surface that exhibits minimal optical interference from reflected light and fingerprints. This combination of properties for hand-held display devices, high compressive surface DOL glass coated to be amphiphobic and also anti-reflective due to the presence of an anti-reflective coating, has not been met by other glass materials used in such devices.
• Figure 3 specifically illustrates an alkali aluminosilicate glass article 100 having a surface compressive layer 104 formed by ion-exchange, a compressive strength of at least 200MPa, a non-ion-exchanged middle portion 106, an anti -reflective coating 110 and a amphiphobic fluorine-based surface layer 102.
• the surface compressive layer 104 has a depth in the range of 20-70 ⁇ m.
• the glass article, exclusive of the antireflective layer 110 and the fluorine-based surface layer 102, has a thickness comprised of the ion-exchanged layer(s) 104 and the middle layer 106. In some embodiments the thickness is at least 0.3 mm.
• the anti-reflective coating layer 110 is comprised of at least one layer and has a thickness in the range of 10-70 ⁇ m. When the antireflective coating is comprised of two or more layers the total thickness of the anti-reflective coating is also in the range of 10-70 ⁇ m.
• the fluorine-based amphiphobic layer typically has a thickness in the range of 1-10 nm, preferably in the range of 1-4 run. In one embodiment the amphiphobic coating has a thickness in the range of 1-2 nm. When a single anti-reflective layer is used the coating material is SiO 2 or F-SiO 2 .
• the layer closest to layer 104 is a metal oxide layer selected from the group HfO 2 , TiO 2 , ZrO 2 , Y 2 O 3 , Gd 2 O 3 , and other metal oxides known in the art to be useful for anti-reflective coatings, and the top layer is SiO 2 or F-SiO 2 .
• the topmost layer is SiO 2 or F-SiO 2 and the antireflective coating layers between the top SiO 2 or F-SiO 2 layer and layer 104 can be any of the foregoing anti-reflective coating materials in any order, though in preferred embodiments the first layer is a metal oxide layer.
• a 3-layer coating can be glass- Y 2 O 3 -TiO 2 -SiO 2 .
• the chemically strengthened, anti-reflective, amphiphobic glass has the following advantages over present commercially available cover glasses.
• the anti-reflective coating applied to the base glass prior to treatment with a fluorine containing amphiphobic-imparting moiety acts to present optical interference due to reflection, thus eliminating glare.
• the anti-reflective coating is versatile and its performance includes controlling the angle of optical interference (or visibility) and thus provides an option for a "privacy" effect by means of structuring a multi-layer coating that enhances this effect.
• the resulting surface is non-polar, minimizing hydrogen (that is, Van der Walls) bonding between foreign particles and oils and the treated glass surface.
• the resulting treated surface has a very low surface energy and a low coefficient of friction.
• the effect and performance of the placement of fluorine-containing moieties as the final "coating" is of added benefit to anti-reflection coatings and surfaces because the elimination of glare means that any noticeable fingerprints become he only source of optical interference, and these can be wiped away.
• Fingerprint removal is typically carried out under either wet or dry conditions by wiping the surface with a cloth. These cloths are often reused and contain dirt and particles that scratch the surface.
• the fluorinated surface enhances the ease of fingerprint removal while minimizing smudges and reducing the number and frequency of events that cause damage which in turn can lead to either immediate or pre-mature failure through fracturing of the glass.
• the scratch resistance of the glass is also improved.
• the high hardness of the chemically strengthened glass and its high compressive surface DOL (for example, 30-80 ⁇ m deep) work to both prevent damage and prevent failure from damage that might occur through repeated wiping. Scratch resistance was then measured using a glass article one-half of which was coated with an amphiphobic coating and the other half uncoated. Scratching was performed as described above. Haze was then measured on both areas on both sides of the article, where haze is a measure of optical clarity in terms scattered light versus the sum of all scattered and transmitted light.
• the coefficient of kinetic friction, ⁇ 5 was also measured. An 80% reduction in friction was found for the coated side versus the uncoated side.
• the surface of a chemically strengthened glass is surface activated by acid treatment prior to application of an amphiphobic coating.
• a pristine drawn glass is chemically strengthened by ion-exchange to a depth of at least 30 ⁇ m using cations larger than the cations in the as-drawn glass.
• cations larger than the cations in the as-drawn glass.
• Na or Li ions a drawn glass can be ion-exchanged using K ion. This exchange imparts a compressive strength to the glass as has been explained above.
• the chemically strengthened glass has a surface that is rich in potassium ions and it is believed that this limits the Si-OH active surface sites to which an amphiphobic coating can be covalent attached, thus inhibiting the bonding of an amphiphobic material such as R F C(O)CI, (Rp) 2 SiCl 2 or (Rp) 3 SiCl, or other coating materials, to the glass surface. It has been found that acid treatment of the ion-exchanged glass prior to application of the amphiphobic coating enhances the adhesion of the amphiphobic coating to the glass and improves both the wettability and wipability of the glass.
• the acid treatment is carried out such that the ions that have been chemically exchanged into the glass are removed to a selected depth, a depth whereby the mechanical performance of the chemically strengthened glass (for example, strength, scratch resistance, impact damage resistance) is not affected.
• the ion-exchange of K ions for Na and/or Li ions is carried out such that the exchange is accomplished to a depth of at least 20 ⁇ m, preferably to a depth in the range of 30-80 ⁇ m.
• the acid treatment is carried out such that only K ions near the surface of the ion-exchanged glass are removed, typically to a depth in the range of ⁇ 50 nm.
• the acid treatment removes the exchanged ion (K ions exchanged for Na and/or Li ions in the base glass) to a depth in the range of 5- 15 nm (0.005-0.015 run).
• K ions exchanged for Na and/or Li ions in the base glass removes the exchanged ion (K ions exchanged for Na and/or Li ions in the base glass) to a depth in the range of 5- 15 nm (0.005-0.015 run).
• a glass 0.3 mm (300 ⁇ m) thick is ion-exchanged by immersion in an ion-exchange bath using K ions as the exchanging ion for Na and/or Li ions, the immersion being for a sufficient time such that ion-exchange is carried out to a depth of 50 ⁇ m with K ions replacing the Na and/or Li ions.
• the resulting exemplary glass viewed through its thickness on the side, would have two surface ion-exchanged layers of 50 nm thickness and a non-exchanged layer of 200 ⁇ m sandwiched between the two ion-exchanged layers. Acid treatment is then carried out such that the exchanged K ions are removed to a depth of 10 nm (0.01 ⁇ m), a depth that does not effect the mechanical performance of the glass.
• the glass After acid treatment the glass, viewed from one face to another through its thickness, has a first 0.01 ⁇ m non-K layer, a first 49.9 ⁇ m K-exchanged layer, a 200 ⁇ m non-exchanged central layer, a second 49.9 ⁇ m K-exchanged layer and an second 0.01 ⁇ m non-K layer.
• one side of the ion-exchanged glass can be covered with a protective layer and acid treated such that K-ions are removed from only one side. After removal of the K-ions, one K-ion removed side is coated with an amphiphobic coating or it can be coated with an anti-reflective coating followed by coating with an amphiphobic coating.
• the acids used in treating the glass are generally strong acids, for example without limitation, sulfuric acid, (H 2 SO 4 ), hydrochloric acid (HCl), perchloric acid (HClO 4 ), nitric acid (HNO 3 ), and other strong acids known in the art. Additional acids that can be used are phosphoric acid (H 3 PO 4 ), acetic acid (CH 3 COOH) and perfluoroacetic acid (CF 3 COOH).
• Figure 4 is a schematic illustrating the generic process flow for preparing glass surfaces for coating with an amphiphobic layer, including an acid treating step, if desired, and also for inspecting and testing the integrity and durability of the amphiphobic coating.
• acid treatment was carried out using 0.3 - 0.5 molar sulfuric acid solution for a time in the range of 5 - 15 minutes at room temperature (approximate range of range of 18-30 °C).
• Table 1 shows the performance data for commercially available Corning Code 1317 glass coated the alkoxysilyl perfluoropolyether DC2604 [an (R f ) n SiX 4-11 compound as described herein], with and without acid treatment as described therein.
• the contact angles were measured for both water and sebaceous oil (used as substitute for actual fingerprint oil). While the contact angle for both was found to increase after acid treatment, the durability of the coating, as determined by wiping tests using a reciprocating wear test machine using a load of -1.5 PSI and up to 10,000 wipe passes, was not adversely affected by the acid treatment.
• Acid treatment is a 10 minute soak in 0.367M H 2 SO 4 at -21 0 C
• Sebaceous oil is also called fingerprint oil.
• Figure 5A illustrates the wiping performance to reduce haze and thus improve optical clarity for CC 1317 glass coated with DC 2604 versus non-coated glass. Initially both surfaces exhibited negligible haze ( ⁇ 0.03%, not illustrated). After coating with fingerprint oil (0 wipes) the haze for both coated and non-coated surfaces was approximately the same (-3.8% and 4%, respectively). However, after wiping the coated glass shows a much faster recovery of optical clarity (haze reduction) than does the non-coated glass. After the 6 th wipe the coated glass exhibits complete recovery (arrow 162 indicating no measurable haze) whereas the non-coated glass still shows -0.5% haze (arrow 160).
• Figure 5B is a photograph of the glass of Figure 5 A after it has undergone the 6 th wipe. The glass is held above the background by means of a clamp at the left (unnumbered).
• numeral 160 represents the uncoated side and numeral 162 represents the coated side, with the line of numeral 164 designating the separation between the two sides.
• Figure 5C is a photograph of a glass that has been abraded across its entire face using 150 grit sandpaper.
• numeral 160 shows abrasion on the uncoated side due to the sandpaper whereas coated side 160 shows no abrasion and remains clear.
• Numeral 164 indicates the separation between the two sides and the glass is held above the background by means of a clamp on the left (unnumbered).
• Figure 6 illustrates the haze (loss of optical clarity) generated by abrasion with 150 grit sandpaper using coated glass and non-coated glass.
• the sample was then abraded across both the coated and non-coated surfaces.
• the data indicates that the non-coated surface had -9.8% haze and the coated surface has - 1.76% haze, respectively. Coating thus represents a 75% reduction in haze generated by scratching damage over the non-coated surface.
• the even numerals 210-226 have the meanings as shown in Table 3.
• Figure 7 Illustrates the kinetic coefficient of friction, ⁇ ⁇ , of CC 1317, DC 2604 coated and non-coated surfaces.
• the friction testing was carried out using "ball-on-flat" sliding contact with a sapphire ball and a steady speed of 20 mm/s with and increasing load of 0.2 to 15.4 grams over a 2.0 mm distance.
• the data indicates that use of the coating results in >60% reduction in ⁇ K over the non-coated glass.
• Figure 8 is a bar chart for a chemically strengthened CC 1317 glass sample one-half of which was treated with acid (standing in 0.35 sulfuric acid solution) and one-half not acid treated. After acid treatment the glass was rinsed and plasma treated and then the entire surface was coated with an amphiphobic coating followed by treatment with fingerprint oil after the coating was cured (50/50 curing). The data at 0 wipes shows haze levels of 17% and ' 14% for the non-coated and coated surfaces, respectively, A single wipe decreases the haze to ⁇ 1.3% and 1% for the uncoated and coated surfaces, respectively, Two wipe reduces the haze for the uncoated surface to ⁇ 0.2% and 0% for the coated surface. These results indicated that acid treatment prior to coating with an amphiphobic material greatly improves the wiping performance which improvement is believed due to increased adherence of the amphiphobic coating to the surface of the glass.
• the coated cover plates as described herein had a sliding angle of less than 10 c for fluid substances placed thereon.
• Table 2 shows the contact angles and sliding angles for water, hexadecane and sebaceous oil for glass surfaces having a perfluorocarbon coating as described herein. The contact angles varied between 115° and 65° according to substance and the sliding arranged from 1° to 9° according to the substance. .
• the contact angle is defined as the angle on the liquid side of the tangential line drawn through the three phase boundary when a liquid, gas and solid intersect.
• the contact angle is a quantitative measure of the wetting of a solid by a liquid and there are commercially available instruments for measuring contact angles. Contact angles are generally measured for non-stick coatings to estimate their surface energy. Using water as an example, when the surface energy is low the contact angle is high, meaning that the liquid does not wet the surface.
• the "sliding angle" of a liquid droplet on a solid surface can also be determined.
• back-side (or device component side) protection for the glass articles of the invention is provided during the processes described herein.
• Back-side protection protects the side of the glass that will not be “touched” by the user of an article having an amphiphobic, chemically strengthened glass cover face as has been described herein. Since the back-side of the glass will not be touched, but will be adjacent to the components in which the cover glass is used, coating is not necessary.
• Backside protection can be accomplished by the use of use of "tapes or films” or “paper/non-adhesive films” which are applied to the glass.
• the "tape or film” process uses a laminate material that is both resistant to dissolution during the amphiphobic coating process and is removable in alcohols (methanol, ethanol, isopropanol, etc.) or ketones (acetone, methyl ethyl ketone and similar ketonic solvents).
• Acrylic adhesive laminates are exemplary materials that can be applied as films and used to protect one side during dip or thermal evaporation techniques and which are resistant to the amphiphobic coating, but the adhesive layer is soluble in acetone.
• Polyimides, polyesters, polyethylenes and polyethylene terephthalate (PET) are examples of tape/film backing materials and then coupled with an acrylic adhesive or modified acrylic adhesive they can be applied to the backside of the glass.
• the tapes/films have an adhesive on one side which permits the tape to be removed after application of the amphiphobic coating to the front or user side of the glass article.
• Preferred are tapes/films that can be die cut and laminated to the glass surface using a commercial laminator. After the backside-protected glass article has been coated with the amphiphobic coating the tape is removed, for example, by peeling. After the tape has been removed any residual adhesive is removed by application of an appropriate solvent that removes the adhesive without affecting the amphiphobic coating. Typically the coating is not soluble in the same solvents that will remove the tape residue.
• Paper/non-adhesive films can also be used for backside protection. For example, dry or wet paper or can be pressed between two articles prior to, for example, dipping the parts into a bath containing the amphiphobic coating.
• a preferred method is to lay the paper (preferably wetted by a liquid that does not contain the amphiphobic material) on a surface and lay the glass article on top of the paper.
• the amphiphobic coating is then applied to the exposed surface of the article.
• the use of a wetted paper prevents the amphiphobic coating from passing between the glass and the paper.

Landscapes

• Chemical & Material Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Engineering & Computer Science (AREA)
• Chemical Kinetics & Catalysis (AREA)
• General Chemical & Material Sciences (AREA)
• Geochemistry & Mineralogy (AREA)
• Materials Engineering (AREA)
• Organic Chemistry (AREA)
• Glass Compositions (AREA)
• Surface Treatment Of Glass (AREA)

Priority Applications (3)

Applications Claiming Priority (4)

Publications (1)

Family

ID=40931968

Family Applications (1)

Country Status (6)

Cited By (35)

Families Citing this family (165)

Citations (6)

Family Cites Families (21)

• 2009
  • 2009-02-05 KR KR1020107019564A patent/KR20100125279A/ko not_active Ceased
  • 2009-02-05 US US12/366,267 patent/US20090197048A1/en not_active Abandoned
  • 2009-02-05 EP EP09708945.2A patent/EP2252557A4/en not_active Withdrawn
  • 2009-02-05 CN CN2009801045736A patent/CN101939266A/zh active Pending
  • 2009-02-05 WO PCT/US2009/000722 patent/WO2009099615A1/en not_active Ceased
  • 2009-02-05 JP JP2010545870A patent/JP2011510904A/ja active Pending

Patent Citations (6)

Non-Patent Citations (1)

Also Published As

Similar Documents

Legal Events