Scratch resistant glass and method of making
09670088 ยท 2017-06-06
Assignee
Inventors
- Sinue Gomez (Corning, NY)
- Robert Michael Morena (Lindley, NY)
- Douglas Miles Noni, Jr. (Horseheads, NY, US)
- James Joseph Price (Corning, NY, US)
- Sara Jean Sick (Beaver Dams, NY, US)
Cpc classification
C03C11/00
CHEMISTRY; METALLURGY
C03C3/087
CHEMISTRY; METALLURGY
Y10T428/315
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
C03C21/002
CHEMISTRY; METALLURGY
C03C2204/00
CHEMISTRY; METALLURGY
C03C15/00
CHEMISTRY; METALLURGY
C03C11/005
CHEMISTRY; METALLURGY
International classification
C03C11/00
CHEMISTRY; METALLURGY
C03C23/00
CHEMISTRY; METALLURGY
C03C15/00
CHEMISTRY; METALLURGY
C03C3/087
CHEMISTRY; METALLURGY
C03C21/00
CHEMISTRY; METALLURGY
Abstract
A scratch resistant alkali aluminoborosilicate glass. The glass is chemically strengthened and has a surface layer that is rich in silica with respect to the remainder of the glass article. The chemically strengthened glass is then treated with an aqueous solution of a mineral acid other than hydrofluoric acid, such as, for example, HCl, HNO.sub.3, H.sub.2SO.sub.4, or the like, to selective leach elements from the glass and leave behind a silica-rich surface layer. The silica-rich surface layer improves the Knoop scratch threshold of the ion exchanged glass compared to ion exchanged glass that are not treated with the acid solution as well as the post-scratch retained strength of the glass.
Claims
1. A glass article comprising SiO.sub.2, wherein the glass article is ion exchanged and has a porous silica-rich region extending from a surface of the glass article to a depth of up to about 600 nm into the article, and wherein the glass article has a Knoop scratch initiation threshold of at least about 12 N.
2. The glass article of claim 1, wherein the glass article has a compressive layer extending from the depth of the silica-rich region to a depth of layer of at least about 20 m, and wherein the layer has a maximum compressive stress of at least about 300 MPa.
3. The glass article of claim 1, wherein the glass article has a Vickers crack initiation threshold of at least about 5 kgf.
4. The glass article of claim 1, wherein the glass article comprises an alkali aluminosilicate glass.
5. The glass article of claim 1, wherein the glass article comprises a borosilicate glass.
6. The glass article of claim 1, wherein the porous silica-rich region of the glass article is acid treated.
7. The glass article of claim 1, wherein the depth of the porous silica-rich region is about 100 nm to about 600 nm.
8. The glass article of claim 1, wherein the Knoop scratch initiation threshold of the glass article is at least about 16 N.
9. The glass article of claim 1, wherein the Knoop scratch initiation threshold of the glass article is about 20 N to about 60 N.
10. A method of making a scratch-resistant glass article, wherein the glass article comprises SiO.sub.2 and is ion exchanged, the method comprising forming a porous silica-rich layer extending from a surface of the glass article to a depth of up to about 600 nm into the article, and wherein the glass article has Knoop crack initiation threshold of at least about 12 N.
11. The method of claim 10, wherein forming the porous silica-rich layer comprises treating the surface with at least one mineral acid other than hydrofluoric acid.
12. The method of claim 11, wherein the at least one mineral acid comprises at least one of HCl, HNO.sub.3, and H.sub.2SO.sub.4.
13. The method of claim 11, wherein the at least one mineral acid is present in a concentration of at least about 0.02 N.
14. The method of claim 13, wherein the at least one mineral acid is present in a concentration in a range from about 0.02 N up to about 60 N.
15. The method of claim 11, wherein forming the porous silica-rich layer comprises treating the surface with the at least one mineral acid at a temperature in a range from about 25 C. up to about 95 C.
16. The method of claim 11, wherein forming the porous silica-rich layer comprises treating the surface with the at least one mineral acid for a time period in a range from about 1 hour up to about 24 hours.
17. The method of claim 10, further comprising forming the ion exchanged glass article prior to forming the silica-rich layer.
18. The method of claim 10, wherein the glass article has a compressive layer extending from the depth of the porous silica-rich layer to a depth of layer of at least about 20 and wherein the compressive layer has a maximum compressive stress of at least about 300 MPa.
19. The method of claim 10, wherein the glass article comprises an alkali aluminosilicate glass.
20. The method of claim 19, wherein the glass article comprises an alkali aluminoborosilicate glass.
21. The method of claim 10, wherein the glass comprises a borosilicate glass.
22. The method of claim 10, wherein the glass article has a Vickers crack initiation threshold of at least about 5 kgf.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
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DETAILED DESCRIPTION
(7) In the following description, like reference characters designate like or corresponding parts throughout the several views shown in the figures. It is also understood that, unless otherwise specified, terms such as top, bottom, outward, inward, and the like are words of convenience and are not to be construed as limiting terms. In addition, whenever a group is described as comprising at least one of a group of elements and combinations thereof, it is understood that the group may comprise, consist essentially of, or consist of any number of those elements recited, either individually or in combination with each other. Similarly, whenever a group is described as consisting of at least one of a group of elements or combinations thereof, it is understood that the group may consist of any number of those elements recited, either individually or in combination with each other. Unless otherwise specified, a range of values, when recited, includes both the upper and lower limits of the range as well as any ranges therebetween. As used herein, the indefinite articles a, an, and the corresponding definite article the mean at least one or one or more, unless otherwise specified. It also is understood that the various features disclosed in the specification and the drawings can be used in any and all combinations thereof.
(8) As used herein, the terms glass article and glass articles are used in their broadest sense to include any object made wholly or partly of glass. Unless otherwise specified, all compositions are expressed in terms of mole percent (mol %) and all temperatures are expressed in degrees Celsius ( C.).
(9) It is noted that the terms substantially and about may be utilized herein to represent the inherent degree of uncertainty that may be attributed to any quantitative comparison, value, measurement, or other representation. These terms are also utilized herein to represent the degree by which a quantitative representation may vary from a stated reference without resulting in a change in the basic function of the subject matter at issue. Thus, a glass that is substantially free of MgO is one in which MgO is not actively added or batched into the glass, but may be present in very small amounts as a contaminant.
(10) Knoop scratch thresholds (KST) described herein are determined using a Knoop diamond indenter. The scratch threshold is determined by first identifying the load range for lateral crack onset. Once the load range is identified, a series of 5 mm long scratches under increasing constant load with three or more scratches per load are generated at a speed of 4 mm/s in order to identify the Knoop scratch threshold. Lateral cracks are defined as sustained cracks that are larger than twice the width of the groove.
(11) Vickers crack initiation thresholds (VIT) described herein are determined by applying and then removing an indentation load to the glass surface at a rate of 0.2 mm/min. The maximum indentation load is held for 10 seconds. The indentation cracking threshold is defined at the indentation load at which 50% of 10 indents exhibit any number of radial/median cracks emanating from the corners of the indent impression. The maximum load is increased until the threshold is met for a given glass composition. All indentation measurements are performed at room temperature in 50% relative humidity.
(12) Compressive stress and depth of layer are measured using those means known in the art. Such means include, but are not limited to, measurement of surface stress (FSM) using commercially available instruments such as the FSM-6000, manufactured by Luceo Co., Ltd. (Tokyo, Japan), or the like, and methods of measuring compressive stress and depth of layer are described in ASTM 1422C-99, entitled Standard Specification for Chemically Strengthened Flat Glass, and ASTM 1279.19779 Standard Test Method for Non-Destructive Photoelastic Measurement of Edge and Surface Stresses in Annealed, Heat-Strengthened, and Fully-Tempered Flat Glass, the contents of which are incorporated herein by reference in their entirety. Surface stress measurements rely upon the accurate measurement of the stress optical coefficient (SOC), which is related to the birefringence of the glass. SOC is in turn measured by those methods that are known in the art, such as fiber and four point bend methods, both of which are described in ASTM standard C770-98 (2008), entitled Standard Test Method for Measurement of Glass Stress-Optical Coefficient, the contents of which are incorporated herein by reference in their entirety, and a bulk cylinder method.
(13) Referring to the drawings in general and to
(14) Although ion exchange provides enhanced surface strength to glass, the improvement in hardness is minimal, and the glass is still susceptible to scratches caused by exposure to materials that are harder than glass. Attempts to improve scratch or abrasion resistance typically include manipulating the composition of the glass itself to increase hardness, use of alternate materials, or applying hard coatings to the glass surface. Compositions may be altered, for example, by minimizing the number of non-bridging oxygen atoms (NBOs) in the glass. Harder materials, such as sapphire or the like, may be used as a substrate or window in lieu of glass, but high processing temperatures, manufacturing processes, and the need for polishing to the desired thickness and shape may be a drawback in terms of scalability and cost. Layers of hard polycrystalline ceramic materials such as sapphire, alumina, diamond-like carbon, and silicon nitrides, carbides, oxycarbides, and the like may be applied to the surface of the glass. In most instances, cost, poor scalability, and loss of transparency makes this approach unsuitable for large area glass applications.
(15) Described herein are scratch-resistant alkali aluminosilicate, alkali aluminoborosilicate, and borosilicate glasses having an integral scratch-resistant layer, A method of forming such a layer and a method of improving the scratch resistance of a glass article are also described. A glass article such as, for example, a sheet or plate, is treated in an acidic aqueous solution at a given temperature for a specified time period. During this process, elements of the glass are selectively removedor leachedleaving behind a porous silica-rich layer extending from the treated surface to a depth within the glass. As used herein, the term silica-rich means that the concentration of silica (SiO.sub.2) in this region is greater than the average silica concentration measured for the bulk of the glass, as a result of the leaching of other components of the glass by the acid treatment. Compared to non-treated glass articles of the same composition, the silica-rich layer improves the scratch resistance of the treated glass surface, as determined by the Knoop scratch threshold, by a factor of 1.5 to 3. In some embodiments, the scratch resistance of the treated glass increases fourfold over that of untreated strengthened glass. In some embodiments, the glass article has a Knoop scratch initiation threshold of at least about 12 Newtons (N) and, in other embodiments, at least about 16 N. In certain embodiments, the Knoop scratch initiation threshold is in a range from about 20 N to about 60 N.
(16) In some embodiments, the glass is chemically strengthened by ion exchange methods that are known in the art. Ion exchange is commonly used to chemically strengthen glasses. In one particular example, alkali cations within a source of such cations (e.g., a molten salt, or ion exchange bath) are exchanged for or replace smaller alkali cations within the glass to achieve a layer that is under a compressive stress (CS) near the surface of the glass. For example, potassium ions from the cation source are often exchanged with sodium ions within the glass. The compressive layer initially extends from the surface to a depth of layer (DOL) within the glass. Following treatment with the aqueous acid solution and formation of the silica-rich layer, the compressive layer extends from the depth of the silica-rich layer to the depth of layer within the glass.
(17) In some embodiments, the compressive stress of the compressive layer has a maximum value of at least about 300 MPa and, in other embodiments, at least about 400 MPa. In certain embodiments, the maximum compressive stress is in a range from about 400 MPa to about 900 MPa. The depth of the compressive layer DOL, in some embodiments, is at least about 20 microns (m) and, in other embodiments, is at least about 30 m. In certain embodiments, the depth of layer is in a range from about 20 m to about 100 m.
(18) The depth or thickness of the scratch-resistant silica-rich layer is typically less than the depth of the compressive layer of the strengthened glass article. In some embodiments, the thickness of the silica-rich layer is about 600 nm or less and, in some embodiments, less than about 100 nm. In other embodiments, the silica-rich layer has a thickness ranging from about 100 nm to about 600 nm.
(19) A cross-sectional schematic view of a planar ion exchanged glass article having a scratch resistant silica-rich surface layer is shown in
(20) Although the surface layers 130, 132 of the acid treated glass is silica-rich and the ion exchanged compressive stress layers 120, 122 comprise additional alkali cations, the compositions of the bulk of the glass articles described herein remain essentially unchanged. The bulk or base glass, in some embodiments, is an alkali aluminosilicate glass. In other embodiments, the bulk or base glass article is an alkali aluminoborosilicate glass. In still other embodiments, the bulk or base glass article is a borosilicate glass that is substantially free of alkali metals and/or oxides thereof.
(21) In some embodiments, the alkali aluminosilicate glass comprises at least about 4 mol % P.sub.2O.sub.5, wherein (M.sub.2O.sub.3(mol %)/R.sub.xO(mol %))<1, where M.sub.2O.sub.3=Al.sub.2O.sub.3+B.sub.2O.sub.3, and wherein R.sub.xO is the sum of monovalent and divalent cation oxides present in the alkali aluminosilicate glass. In some embodiments, the monovalent and divalent cation oxides are selected from the group consisting of Li.sub.2O, Na.sub.2O, K.sub.2O, Rb.sub.2O, Cs.sub.2O, MgO, CaO, SrO, BaO, and ZnO. In certain embodiments, the glass comprises 0 mol % B.sub.2O.sub.3. In some embodiments, the glass is ion exchanged to a depth of layer of at least about 10 m and comprises at least about 4 mol % P.sub.2O.sub.5, wherein 0.6<[M.sub.2O.sub.3(mol %)/R.sub.xO(mol %)]<1.4; or 1.3<[(P.sub.2O.sub.5+R.sub.2O)/M.sub.2O.sub.3]2.3; where M.sub.2O.sub.3=Al.sub.2O.sub.3+B.sub.2O.sub.3, R.sub.xO is the sum of monovalent and divalent cation oxides present in the alkali aluminosilicate glass, and R.sub.2O is the sum of monovalent cation (i.e., alkali) oxides present in the alkali aluminosilicate glass. The glass is described in U.S. patent application Ser. No. 13/678,013 by Timothy M. Gross, entitled Ion Exchangeable Glass with High Crack Initiation Threshold, and U.S. patent application Ser. No. 13/677,805 by Timothy M. Gross, entitled Ion Exchangeable Glass with High Crack Initiation Threshold, both filed Nov. 15, 2012, and claiming priority to U.S. Provisional Patent Application No. 61/560,434 filed Nov. 16, 2011. The contents of these applications are incorporated herein by reference in their entirety.
(22) In other embodiments, the alkali aluminoborosilicate glass comprises: at least about 50 mol % SiO.sub.2; at least about 10 mol % R.sub.2O, wherein R.sub.2O comprises Na.sub.2O; Al.sub.2O.sub.3; and B.sub.2O.sub.3, wherein B.sub.2O.sub.3(R.sub.2OAl.sub.2O.sub.3)3 mol %. In some embodiments, the glass comprises: at least about 50 mol % SiO.sub.2; at least about 10 mol % R.sub.2O, wherein R.sub.2O comprises Na.sub.2O; Al.sub.2O.sub.3, wherein Al.sub.2O.sub.3(mol %)<R.sub.2O(mol %); and from about 3 mol % to about 4.5 mol % B.sub.2O.sub.3, wherein B.sub.2O.sub.3(mol %)-(R.sub.2O(mol %)-Al.sub.2O.sub.3(mol %))3 mol %. In certain embodiments, the glass comprises: at least about 50 mol % SiO.sub.2; from about 9 mol % to about 22 mol % Al.sub.2O.sub.3; from about 3 mol % to about 10 mol % B.sub.2O.sub.3; from about 9 mol % to about 20 mol % Na.sub.2O; from 0 mol % to about 5 mol % K.sub.2O; at least about 0.1 mol % MgO, ZnO, or combinations thereof, wherein 0 mol %MgO6 mol % and 0 mol %ZnO6 mol %; and, optionally, at least one of CaO, BaO, and SrO, wherein 0 mol %CaO+SrO+BaO2 mol %. When ion exchanged, the glass, in some embodiments, has a Vickers crack initiation threshold of at least about 10 kgf. Such glasses are described in U.S. patent application Ser. No. 14/197,658, filed May 28, 2013, by Matthew J. Dejneka et al., entitled Zircon Compatible, Ion Exchangeable Glass with High Damage Resistance, which is a continuation of U.S. patent application Ser. No. 13/903,433, filed May 28, 2013, by Matthew J. Dejneka et al., entitled Zircon Compatible, Ion Exchangeable Glass with High Damage Resistance, both claiming priority to Provisional Patent Application No. 61/653,489, filed May 31, 2012. The contents of these applications are incorporated herein by reference in their entirety.
(23) In some embodiments, the alkali aluminoborosilicate glass comprises: at least about 50 mol % SiO.sub.2; at least about 10 mol % R.sub.2O, wherein R.sub.2O comprises Na.sub.2O; Al.sub.2O.sub.3, wherein 0.5 mol %Al.sub.2O.sub.3R.sub.2O2 mol %; and B.sub.2O.sub.3, and wherein B.sub.2O.sub.3(R.sub.2O(mol %)-Al.sub.2O.sub.3)4.5 mol %. In other embodiments, the glass has a zircon breakdown temperature that is equal to the temperature at which the glass has a viscosity of greater than about 40 kPoise and comprises: at least about 50 mol % SiO.sub.2; at least about 10 mol % R.sub.2O, wherein R.sub.2O comprises Na.sub.2O; Al.sub.2O.sub.3; and B.sub.2O.sub.3, wherein B.sub.2O.sub.3(R.sub.2OAl.sub.2O.sub.3)4.5 mol %. In still other embodiments, the glass is ion exchanged, has a Vickers crack initiation threshold of at least about 30 kgf, and comprises: at least about 50 mol % SiO.sub.2; at least about 10 mol % R.sub.2O, wherein R.sub.2O comprises Na.sub.2O; Al.sub.2O.sub.3, wherein 0.5 mol %Al.sub.2O.sub.3R.sub.2O2 mol %; and B.sub.2O.sub.3, wherein B.sub.2O.sub.3(R.sub.2OAl.sub.2O.sub.3)4.5 mol %. Such glasses are described in U.S. patent application Ser. No. 13/903,398, by Matthew J. Dejneka et al., entitled Ion Exchangeable Glass with High Damage Resistance, filed May 28, 2013, claiming priority from U.S. Provisional Patent Application No. 61/653,485, filed May 31, 2012. The contents of these applications are incorporated by reference herein in their entirety.
(24) In other embodiments the alkali aluminosilicate glass comprises: from about 70 mol % to about 80 mol % SiO.sub.2; from about 6 mol % to about 12 mol % Al.sub.2O.sub.3; from about 0 mol % to about 15 mol % B.sub.2O.sub.3; from about 0 mol % to about 15 mol % Li.sub.2O; from about 0 mol % to about 20 mol % Na.sub.2O; from about 0 mol % to about 10 mol % K.sub.2O; from about 0 mol % to about 8 mol % MgO; from about 0 mol % to about 10 mol % CaO; from about 0 mol % to about 5 mol % each of ZnO, ZrO.sub.2, and Fe.sub.2O.sub.3; and from 0 mol % to about 1 mol % each of SnO.sub.2 and P.sub.2O.sub.5. In some embodiments, SiO.sub.2+B.sub.2O.sub.3+Al.sub.2O.sub.386.5 mol % and R.sub.2OROAl.sub.2O.sub.3<5 mol %; and, in other embodiments, SiO.sub.2+B.sub.2O.sub.3+Al.sub.2O.sub.386.5 mol % and R.sub.2OROAl.sub.2O.sub.3<5 mol %. Such glasses are described in U.S. Provisional Patent Application No. 61/987,795, filed May 2, 2014, by Jeffrey Scott Cites et al., entitled Strengthened Glass and Compositions Therefor, the contents of which are incorporated by reference herein in their entirety.
(25) In some embodiments, the alkali aluminosilicate and alkali aluminoborosilicate glasses described hereinabove are substantially free of (i.e., contain 0 mol %) of at least one of lithium, boron, barium, strontium, bismuth, antimony, and arsenic.
(26) In some embodiments, the alkali aluminosilicate glasses described hereinabove are down-drawable by processes known in the art, such as slot-drawing, fusion drawing, re-drawing, and the like, and may have liquidus viscosities of at least 130 kilopoise.
(27) In other embodiments, the glass is a borosilicate glass such as, for example, Corning Eagle XG glass, manufactured by Corning Incorporated.
(28) In another aspect, a method of increasing the scratch resistance of a chemically strengthened glass article is provided. A porous silica-rich layer is formed on the surface of the glass article. The silica-rich layer extends from the surface of the glass article to a depth of up to about 600 nm or less and, in some embodiments, less than about 400 nm. In other embodiments, the silica-rich layer has a thickness ranging from about 100 nm to about 600 nm. The glass article, in some embodiments, is treated with an aqueous solution comprising at least one mineral acid such as, but not limited to hydrochloric (HCl), nitric (HNO.sub.3), sulfuric (H.sub.2SO.sub.4), combinations thereof, or the like. The aqueous acid solution, in some embodiments, has an acid concentration ranging from about 0.005 normal (N) to about 1.0 N. In one particular embodiment, the acid concentration of the solution is about 0.2 N. In some embodiments, the aqueous acid solution is substantially free of or does not contain hydrofluoric acid (HF). During this process, other elements present in the glass (e.g., alkalis, alkaline earths, aluminum, boron, phosphorus, etc.) are selectively leached out of the affected area, leaving behind the silica-rich layer, which is integral to the glass article. The porous silica-rich layer improves the scratch resistance, as characterized by the Knoop scratch threshold, of the glass surface. The at least one mineral acid is applied to the surface to be treated by those means known in the art, such as immersion, dipping, spraying, brushing, spinning, or the like. The aqueous solution comprising the at least one mineral acid is allowed to stay in contact with the surface for a time sufficient to form a silica-rich layer having a desired depth or thickness. The actual time required needed to achieve a desired depth or thickness of the layer depends on multiple factors, including concentration of the aqueous acid solution, temperature of the substrate and/or acid solution, glass composition, and the like.
(29) The acid treatment of the chemically strengthened glass article with the aqueous acid solution takes place at a predetermined or selected temperature. In some embodiments, the glass article and/or the solution are heated at a temperature ranging from about 25 C. to about 95 C. In other embodiments, the glass article and/or the solution are heated at a temperature ranging from about 50 C. to about 95 C. The glass article, for example, may be at room temperature, while the aqueous acid solution is heated to the desired temperature. Alternatively, both the glass article and the aqueous solution may be preheated prior to treatment.
(30) The method described herein results in up to a four-fold improvement in the scratch resistance of ion-exchangeable glasses. In some embodiments, the glasses treated in accordance with this method exhibit up to a four-fold improvement in scratch-resistance compared that strengthened samples of identical composition that are not treated (non-treated). In some embodiments, the acid treatment of the samples tested involves exposure of a glass plate to an aqueous solution of 0.02N H.sub.2SO.sub.4 or 1 molar (M) HNO.sub.3 at 95 C. for 24 hours. During acid exposure, elements of the glass are selectively leached, leaving behind a silica-rich surface layer (e.g., 130, 132 in
(31) Scratch resistance of selected glasses was evaluated using a Knoop diamond indenter. The scratch threshold is determined by first identifying the load range for lateral crack onset. Once the load range is identified, a series of 5 mm long scratches under constant load are generated at a speed of 4 mm/s Scratches are made under increasing load, with three or more scratches per load, in order to identify the Knoop scratch threshold. Lateral cracks are defined as sustained cracks that are greater than twice the width of the groove.
(32) Results of Knoop scratch threshold measurements for glass compositions tested after ion exchange (IX), and after ion exchange followed by the acid treatment described herein are plotted in
(33) TABLE-US-00001 TABLE 1 Compositions glasses and Knoop scratch threshold (KST) data obtained for ion exchanged glasses with and without subsequent acid treatment acid. Mol % A B C D E F SiO.sub.2 69.2 64.4 64.7 68.8 67.4 Al.sub.2O.sub.3 8.5 13.9 13.9 10.6 12.7 B.sub.2O.sub.3 0.0 7.2 5.1 0.0 3.7 Li.sub.2O 0.0 0.0 0.0 0.0 0.0 Na.sub.2O 13.9 14.0 13.8 14.9 13.7 K.sub.2O 1.2 0.5 0.0 0.0 0.0 MgO 6.5 0.0 2.4 5.4 2.4 ZnO 0.0 0.0 0.0 0.0 0.0 CaO 0.5 0.1 0.1 0.0 0.0 P.sub.2O.sub.5 0.0 0.0 0.0 0.0 0.0 SnO.sub.2 0.2 0.1 0.1 0.2 0.1 Knoop Scratch Threshold (N) ion- 4-6N 8-10N 8-12N 4-5N 8-12N 10-12N exchanged glass IX + 0.02N 6-8N 18-20N 20-22N H.sub.2SO.sub.4 @95 C. 24 h IX + 1M 18-20N HNO.sub.3 @95 C. 24 h
(34) TABLE-US-00002 TABLE 2 Compositions glasses and Knoop scratch threshold (KST) data obtained for ion exchanged glasses with and without subsequent acid treatment acid. Mol % 1 2 3 4 5 6 7 8 SiO.sub.2 70.1 70.1 70.1 70.1 73.0 72.0 70.0 70.5 Al.sub.2O.sub.3 10.0 10.0 10.0 10.0 9.2 9.3 10.0 10.3 B.sub.2O.sub.3 6.3 4.3 6.3 8.4 7.1 7.4 7.9 8.0 Li.sub.2O 0.0 0.0 0.0 0.0 0.5 0.5 0.5 0.5 Na.sub.2O 11.2 11.2 9.2 9.2 9.7 10.3 11.1 10.2 K.sub.2O 0.2 0.2 2.2 2.2 0.5 0.5 0.5 0.5 MgO 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 ZnO 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 CaO 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 P.sub.2O.sub.5 2.0 4.0 2.0 0.0 0.0 0.0 0.0 0.0 SnO.sub.2 0.1 0.1 0.1 0.1 0.1 0.1 0.1 0.1 Knoop Scratch Threshold (N) ion- 16-18N 14-16N 16-18N 16-18N >40N 18-20N 12-14N 14-16N exchanged glass IX + 0.02N 40-44N 54-56N 42-44N 48-50N 26-28N 22-24N 20-22N 22-24N H.sub.2SO.sub.4 @95 C. 24 h IX + 1M 38-40N 22-24N 26-28N 38-40N HNO.sub.3 @95 C. 24 h
(35)
(36) Increased hardness is typically regarded as the solution for improving scratch resistance of glass surfaces. Hardness usually scales linearly with elastic modulus.
(37) While typical embodiments have been set forth for the purpose of illustration, the foregoing description should not be deemed to be a limitation on the scope of the disclosure or appended claims. Accordingly, various modifications, adaptations, and alternatives may occur to one skilled in the art without departing from the scope of the present disclosure or appended claims.