MXPA98006312A - Lead-free glass composition, low temperat fusion - Google Patents
Lead-free glass composition, low temperat fusionInfo
- Publication number
- MXPA98006312A MXPA98006312A MXPA/A/1998/006312A MX9806312A MXPA98006312A MX PA98006312 A MXPA98006312 A MX PA98006312A MX 9806312 A MX9806312 A MX 9806312A MX PA98006312 A MXPA98006312 A MX PA98006312A
- Authority
- MX
- Mexico
- Prior art keywords
- glass
- composition
- enamel
- consists essentially
- frit
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 86
- 239000011521 glass Substances 0.000 title claims abstract description 78
- 230000004927 fusion Effects 0.000 title description 2
- 210000003298 Dental Enamel Anatomy 0.000 claims abstract description 50
- 238000002844 melting Methods 0.000 claims abstract description 6
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims abstract description 6
- KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000000758 substrate Substances 0.000 claims description 24
- 239000000463 material Substances 0.000 claims description 13
- 239000000049 pigment Substances 0.000 claims description 11
- 239000007787 solid Substances 0.000 claims description 10
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims description 6
- 229910052797 bismuth Inorganic materials 0.000 claims description 6
- BPQQTUXANYXVAA-UHFFFAOYSA-N silicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims description 4
- WMWLMWRWZQELOS-UHFFFAOYSA-N Bismuth(III) oxide Chemical compound O=[Bi]O[Bi]=O WMWLMWRWZQELOS-UHFFFAOYSA-N 0.000 abstract description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 5
- 229910052681 coesite Inorganic materials 0.000 abstract description 2
- 229910052906 cristobalite Inorganic materials 0.000 abstract description 2
- 229910052904 quartz Inorganic materials 0.000 abstract description 2
- 239000000377 silicon dioxide Substances 0.000 abstract description 2
- 229910052682 stishovite Inorganic materials 0.000 abstract description 2
- 230000035882 stress Effects 0.000 abstract description 2
- 239000000126 substance Substances 0.000 abstract description 2
- 229910052905 tridymite Inorganic materials 0.000 abstract description 2
- 235000010215 titanium dioxide Nutrition 0.000 abstract 2
- 239000006059 cover glass Substances 0.000 abstract 1
- NTGONJLAOZZDJO-UHFFFAOYSA-M disodium;hydroxide Chemical compound [OH-].[Na+].[Na+] NTGONJLAOZZDJO-UHFFFAOYSA-M 0.000 abstract 1
- 235000012239 silicon dioxide Nutrition 0.000 abstract 1
- 239000000919 ceramic Substances 0.000 description 9
- 238000010411 cooking Methods 0.000 description 8
- 239000000843 powder Substances 0.000 description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- 239000011159 matrix material Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000005755 formation reaction Methods 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- 229910000416 bismuth oxide Inorganic materials 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- -1 cobalt chromium iron Chemical compound 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 238000007639 printing Methods 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
- BERDEBHAJNAUOM-UHFFFAOYSA-N Copper(I) oxide Chemical compound [Cu]O[Cu] BERDEBHAJNAUOM-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N ZrO2 Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 239000005328 architectural glass Substances 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium monoxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000002320 enamel (paints) Substances 0.000 description 2
- 230000002708 enhancing Effects 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- 238000010304 firing Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 238000007496 glass forming Methods 0.000 description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- 239000006060 molten glass Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- XFRVVPUIAFSTFO-UHFFFAOYSA-N 1-Tridecanol Chemical compound CCCCCCCCCCCCCO XFRVVPUIAFSTFO-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N AI2O3 Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N Boron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 description 1
- JHLNERQLKQQLRZ-UHFFFAOYSA-N Calcium silicate Chemical class [Ca+2].[Ca+2].[O-][Si]([O-])([O-])[O-] JHLNERQLKQQLRZ-UHFFFAOYSA-N 0.000 description 1
- JGDFBJMWFLXCLJ-UHFFFAOYSA-N Copper chromite Chemical compound [Cu]=O.[Cu]=O.O=[Cr]O[Cr]=O JGDFBJMWFLXCLJ-UHFFFAOYSA-N 0.000 description 1
- BWFPGXWASODCHM-UHFFFAOYSA-N Copper monosulfide Chemical compound [Cu]=S BWFPGXWASODCHM-UHFFFAOYSA-N 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L Copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- 206010018987 Haemorrhage Diseases 0.000 description 1
- FUJCRWPEOMXPAD-UHFFFAOYSA-N Lithium oxide Chemical compound [Li+].[Li+].[O-2] FUJCRWPEOMXPAD-UHFFFAOYSA-N 0.000 description 1
- 229920000914 Metallic fiber Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive Effects 0.000 description 1
- 235000013361 beverage Nutrition 0.000 description 1
- 230000000740 bleeding Effects 0.000 description 1
- 231100000319 bleeding Toxicity 0.000 description 1
- 229910052810 boron oxide Inorganic materials 0.000 description 1
- 230000001680 brushing Effects 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N chromium Chemical group [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 239000001031 chromium pigment Substances 0.000 description 1
- 229910052803 cobalt Inorganic materials 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- 229940112669 cuprous oxide Drugs 0.000 description 1
- 230000004059 degradation Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000010433 feldspar Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 239000005337 ground glass Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229910052909 inorganic silicate Inorganic materials 0.000 description 1
- 229910001416 lithium ion Inorganic materials 0.000 description 1
- 229910001947 lithium oxide Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000035800 maturation Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M methacrylate group Chemical group C(C(=C)C)(=O)[O-] CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 229910003455 mixed metal oxide Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000003211 photoinitiator Substances 0.000 description 1
- 230000019612 pigmentation Effects 0.000 description 1
- 239000010665 pine oil Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 150000004763 sulfides Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- JPJZHBHNQJPGSG-UHFFFAOYSA-N titanium;zirconium;tetrahydrate Chemical compound O.O.O.O.[Ti].[Zr] JPJZHBHNQJPGSG-UHFFFAOYSA-N 0.000 description 1
- 229940087291 tridecyl alcohol Drugs 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Abstract
The present invention relates to: low melting lead-free glass compositions, glass frits consisting of said composition and glass enamels made therefrom for cover glass, especially automotive glassware. The composition consists of (% by weight): 45-67% Bi2O3, 24-39% SiO2, 8 ~ -10% B203, 1-7% ~ Na2O, 0.5% A1203, 0-4% TiO2, 0, 3% TiO2, 0.3% Li2.0, 0.4% F-1. The glass composition exhibits good chemical durability and good anti-tack properties and avoids stresses in the cast enamel
Description
COMPOSITION OF LEAD-FREE GLASS, LOW TEMPERATURE FUSION
This invention relates to low temperature melting lead-free glass compositions.
BACKGROUND OF THE INVENTION Lead-free glass compositions are known in the art. Illustrative are the following: Reinherz U.S. Patent No. 4,892,847 Francel U.S. Patent No. 4,554,258 Roberts U.S. Patent No. 5,252,521 Klimas U.S. Patent No. 4,970 .178 Clifford U.S. Patent No. 5,308,803 Murkens U.S. Patent No. 5,093,285 Ryan U.S. Patent No. 5,559,059 Ne man U.S. Patent No. 2,301,100 Can be formed additional discoveries of lead-free glass compositions in Francel et al., U.S. Patent No. 4,446,241, Francel et al., U.S. Patent No. 4,537,862, Reade, U.S. Patent No. 4,224 .074, Eppler, U.S. Patent No. 4,312,951, Eppler, REF .: 28035 U.S. Patent No. 4,376,169, Emlemdi, U.S. Pat. No. 5,504,045, Manaba et al. U.S. Patent No. 5,578,533 and Evans and others, Inter Application National No. PCT / EP94 / 00403. These glass compositions are generally used to form, in a well-known manner, glass frits which are in turn used to formulate glass enamel compositions. These glass enamel (or ceramic) compositions are known as useful for the formation of decorative coatings for glassware, porcelain articles, architectural glasses and the like. They are especially useful in forming colored edges around glass sheets used for automotive windshields, side lights and taillights. These colored edges enhance the appearance as well as prevent the UV degradation of the fundamental adhesives. In general, these enamel compositions consist essentially of a glass frit, a colorant and an organic carrier. They are applied to a desired substrate and subsequently ignited to burn the organic vehicle and melt the frit, thereby bonding the enamel coating to the substrate.
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Glass sheets for automotive use are generally coated with the ceramic enamel composition, and then subjected to a process of formation at elevated temperatures. During this treatment the enamel is fused and melted to the glass substrate, and the final desired shape is given to the glass. However, many prior art coatings exhibit a tendency to adhere to the materials covering the forming matrix, such as a matrix covered with metallic fiber or glass fiber, because these conventional glazes have a low viscosity after melting and stick to other materials at high temperature. Accordingly, these materials are not suitable for use in glass forming processes in which the heated enamel-coated glass is contacted with a forming die covered with material. Several approaches have been suggested to facilitate the formation of glass sheets with a ceramic enamel coated thereon, withstanding the high forming or bending temperatures, and the repeated contact of the glass sheet and the covered forming matrix without the enamel will adhere to the forming matrix. For example, U.S. Patent Nos. 4,596,590 and 4,770,685 (issued to Boaz) and EP 201241 propose the addition of a low valence metal oxide powder, eg, cuprous oxide, to the paint composition to provide a non-stick barrier between the coating and the glass fiber-covered forming matrix. U.S. Patent Nos. 4,684,389; 4,857,096 and 5,037,783 (granted to Boaz), propose the addition of finely divided zinc metal powder for a similar effect. The use of a metallic iron powder is proposed in U.S. Patent No. 4,983,196 (issued to Stotka). The use of other metal oxide powders, including formulations containing bismuth oxide, is proposed in U.S. Patent Nos. 4,029,605 (issued to Kosiorek); 4,098,949 (issued to Kosiorek); 4,892,847 (granted to Reinherz), 4,959,090 (granted to (granted to Klimas and others), 5,093,285 (granted to Murkene); 5,203,902 (granted to Murkens) and EP 370,693. bismuth-containing systems produce a weak glass, such as when lithium is present, and have poor silver bleed properties, as well as inadequate anti-scallop properties US Patent No. 4,828,596 proposes the introduction of copper sulphide or copper sulfate in the ceramic enamel composition as an anti-stick agent.Sulfides or sulfates of other metals have been proposed as anti-tack agents in U.S. Patent No. 4,892,396 (issued to Reinherz). U.S. Patent Nos. 5,153,150 and 5,208,191 (issued to Ruderer et al.) Propose a supposedly improved anti-stick ceramic glaze composition, wherein a seed powder containing Zn 2 Si 4 is introduced into an oxide composition with or without the presence of bismuth oxide. As another problem, a number of prior ceramic enamel systems employ a glass frit containing lead. Due to environmental considerations it is desirable to avoid the use of any system containing lead. Furthermore, while some of the enamel systems mentioned above may perform very well in conventional glass-forming processes, some are not satisfactory for use in the newly developed "deep bending" processes for the formation of automotive glass. Each of the previously known enamel compositions suffers from one or more of the deficiencies noted above, making it desirable to provide a composition that avoids these defects. The present invention provides such ceramic enamel compositions, a method for employing the compositions, and substrates coated therewith. The present invention provides a glass and glass frit composition produced therefrom, which can be used in the production of enamels having improved chemical durability properties to the molten enamel coating. Currently, the only lead-free glass frits suitable for automotive enamel use that pass the required sulfuric acid durability evaluation specification, for example, in Japan, use lithium ions. However, if it is not carefully controlled, the use of lithium can cause unwanted stresses and rupture of the substrates. The new glass compositions of this invention avoid this problem. These compositions also impart excellent anti-tack properties,
DESCRIPTION OF THE INVENTION The present invention provides novel glass compositions from which glass frits containing bismuth borosilicate, having a higher boron oxide content and / or higher bismuth oxide, can be obtained. These systems do not require the use of zirconium oxide, titanium oxide or lithium oxide within the range of composition. The glass compositions of the present invention are as follows:
The glass compositions are formed in a known manner, as for example, by combining the known starting materials and fusing at a temperature of about -1000 ° to 1300 ° C for about forty (40) minutes, to form a molten glass having the desired composition. The molten glass formed can then be tempered with water in a known manner to form a frit. The frit can then be milled using conventional grinding techniques, at a fine particle size, preferably between 2 and 6 microns. The invention also provides glass enamel (ceramic) compositions employing the glass frit compositions described above. These compositions comprise from about 25 to 90% by weight solids of a glass frit component. This component comprises the discovered glass frit compositions. This glass frit component can be a unique composition of the invention, or alternatively, it can be a mixture of these frits. Furthermore, at least one frit of the present invention can be combined with an additional low melting frit having a composition outside the scope of those of the invention, to the extent that this other frit does not impair the qualities of the enamel that results. Representatives of said other frit that can be used is one that has a composition that is shown below: Oxide Range% in Weight Si02 20 - 35 - -
Bi203 10 - 50 ZnO 5 - 45 B203 5 - 15 Na20 1 - 7 CaO 0 - 10 Ti02 0 - - 2 A1203 0 - - 5 Zr02 0 • - 2 F2 0 - - 1 A method for making said frit is discovered in the U.S. Patent No. 5,346,651. These frits have a cooking temperature low enough to ensure adequate adhesion to the substrate, and also have low density characteristics. The enamel composition further contains from about 10 to 37% by weight solids of an oxide pigment or combinations of oxide pigments. Such pigments are known in the art and can be obtained commercially. Examples are those such as CuCr20, (Co, Fe) (Fe, Cr) 204 and the like. Illustrative are the pigments that can be obtained from Cerdee Corporation such as pigment * 2991, which is a pigment of black copper chromite, pigment * 2980 which is a pigment of cobalt chromium iron black and pigment * 2987 which It is a chromium black pigment made of nickel manganese iron. The enamel compositions further contain an organic vehicle. The vehicle to be employed in the compositions is selected based on its end-use application. It is essential that the vehicle adequately suspend the particulates and burn completely with the cooking of the composition on the substrate. The vehicles are typically organic, and include compositions based on pine oils, vegetable oils, mineral oils, low molecular weight petroleum fractions, tridecyl alcohol, natural and synthetic resins, and the like. Surfactants and / or other film forming modifiers may also be included. As appropriate, UV-based vehicles are equally applicable for use in the invention. Such UV-based vehicles are well known in the art, and in general are composed of polymerizable monomers and / or oligomers containing, for example, acrylate or methacrylate functional groups, together with photoinitiators and polymerization inhibitors. Representative systems are disclosed in U.S. Patent Nos. 4,306,012 and 4,649,062. How it is recognized, said systems are cured with ultraviolet radiation after application to the substrate. The specific vehicle and the amounts used are selected based on the specific components of the composition and the desired viscosity. In general, the amount of the vehicle is about 10 to about 40% by weight based on the total weight of the enamel composition. In general, the enamel compositions are viscous in nature, the viscosity depending on the method of application to be employed and the end use. For viscosity printing purposes, viscosities ranging from 10 N * s / m2 (10,000 cpoise) to 80 N * s / m2 (80,000 cpoise), and preferably 35 N * s / m2 (35,000 cpoise) to 65 are appropriate. N * s / m2 (65,000 cpoises) at 20 ° C, as determined on a Brookfield Viscometer, needle # 7 at 20 rpm. The enamels of the invention may additionally contain up to about 15% by weight solids of a commonly used filler, such as silica and alumina, and other conventional additives, such as iron, silicon, zinc and the like, to enhance the desired properties, such as resistance to silver bleeding. The filler may also be a refractory oxide filler, such as wollastonite and materials such as alumina-silicate materials, calcium silicate compounds, boron-alumina-silicate compounds, soda-calcium-alumina-silicate compounds, feldspar compounds, titanium and combinations of said oxides. The enamel compositions may also contain up to about 20% by weight solids of a crystalline seed material, such as bismuth silicate, which is disclosed in my co-pending United States Patent Application No. 08 / 569,905, filed on April 8, 1995. December 1995, which is incorporated herein by reference. Bismuth silicate seed materials include, but are not limited to, Bi? 2Si02cw Bi4 (Si04) 3 and Bi2Si05. The enamel compositions will generally contain from about 85 to about 60% by weight solids as described above, and about 15 to about 40% by weight of the suitable organic carrier. The viscosity of the composition is adjusted so that it can be screen printed, roller coated or sprayed onto the desired substrate. The invention further provides a substrate having an enamel composition of the invention fired thereon. Said substrates are illustrated by glass, ceramic or other non-porous substrate, and in particular an automotive glass substrate. Other substrates include architectural glass, appliances and beverage containers.
To prepare the enamel compositions of the invention, the required frit or chips are ground to a fine powder using conventional methods. The frit component is combined with the other solids components and the solids are mixed with the necessary vehicle. The viscosity is adjusted as desired. Once the enamel composition is ready, it can be applied to the substrate in a conventional manner, such as by screen printing, decal application, spraying, brushing, roller coating or the like. Sieve printing is preferred when the composition is applied to a glass substrate. After application of the composition to a substrate in a desired pattern, the applied coating is then baked to bond the enamel to the substrate. The cooking temperature in general is determined by the maturation temperature of the frit, and is preferably in a wide temperature range. Typically, the cooking range for a present composition is in the range of about 500 ° to 750 ° C, more preferably in the range of about 520 ° to 650 ° C, and more preferably about 530 ° to 620 ° C. .
EXAMPLES Low melting glass frit compositions are produced by mixing raw materials that are known in the art, and using methods known to those skilled in the art. The well-mixed raw material batch compositions are then fused at temperatures between 1000 to 1300 ° C, followed by a sudden cooling, again using methods known to those skilled in the art. The glass compositions are then milled to a fine particle size, preferably between 2 and 6 microns, using a ball mill. The finely ground powder frits are then used to form glass enamel compositions. The finely ground glass frit is combined with a mixed metal oxide pigment. In addition, the solids of the enamel compositions are dispersed and suspended in a vehicle selected for the end-use application. The evaluation is carried out by sieving the resulting frit or enamel paste on a microscope slide or automotive glass substrate. The automotive glass slides or substrate are then fired at various temperatures to determine the "cooking temperature", TC, or "minimum cooking temperature" CM. The TC is the temperature when the glass has enough time to flow and melt within a 15 minute firing and produce a smooth, shiny surface. The CM is the temperature where the enamel has enough time to flow and melt in a 4 minute firing and produce an enamel without interconnected porosity.
The preheating time is 10 and 6 minutes at 427 ° C for TC and CM respectively. The acid resistance is evaluated using ASTM C-724-91, using a 10% by weight solution of citric acid. The cooked tests are exposed to the solution for 15 minutes and classified based on the following: Grade 1 - No apparent attack Grade 2 - Iridescence or visible spotting on the exposed surface when viewed at a 45 ° angle, but not apparent when observed at angles less than 30 °. Grade 3 - A defined stain that does not blur the reflected images and is visible at angles less than 30 °. Grade 4 - Spotting defined with a large color change or surface "strongly iridescent visible at angles less than 30 ° and which can blur the reflected images." Grade 5 - Cloudy or matte surface with possible dusting.
- -
Grade 6 - Significant removal of enamel with obvious tiny holes. Grade 7 - Complete removal of enamel in exposed area.
Formulation of glass frit (% by weight)
Next follow black automotive enamel formulations, made with the frit of the examples given above.
Formulation of Black Enamel (% by weight)
* 2991 is a copper chromium pigment and RD-2077 is a bismuth silicate material. Both materials can be obtained commercially from Cerdee Corporation, Drakenfeld Products, West Wylie Avenue, Washington, Pennsylvania. The anti-tack properties are evaluated by printing the enamels on a piece of 10. 15 cm x 10. 15 cm (4"x 4") of automotive glass substrate, cooking in a cooking cycle of the automotive type of 3 to 5 minutes, and pressing with a pad of commercially used material, while the hot enamel and the substrate are kept inside the oven.
It is noted that, in relation to this date, the best method known to the applicant to carry out the aforementioned invention is that which is clear from the present description of the invention.
Having described the invention as above, the content of the following is claimed as property.
Claims (17)
1 . A glass composition, characterized in that it consists essentially of:
2 . A glass composition according to claim 1, characterized in that it consists essentially of:
3 . A glass composition, characterized in that it consists essentially of:
Four . A glass frit produced from a glass composition, characterized in that it consists essentially of: -
5. A glass frit according to claim 4, wherein the glass composition consists essentially of
6. A glass frit according to claim 4, wherein the glass composition consists essentially of
7. A glass frit according to claim 4, characterized in that the glass composition consists essentially of
8. In a glass enamel composition comprising a glass frit component, an oxide pigment component and an organic vehicle, the refinement wherein the glass frit component comprises at least one glass frit produced from a glass composition which consists essentially of
9. A glass enamel composition according to claim 8, wherein the glass composition consists essentially of
10. A glass enamel composition according to claim 8, wherein the glass composition consists essentially of
11. A glass enamel composition according to claim 8, wherein the glass composition consists essentially of A1203 0.3 to 0 by weight Ti02 1.4 a or by weight Na20 4.3 Q.? by weight K; 0 0.6 0, 0 by weight
12. A glass enamel composition according to claim 8, wherein the solids content is about 85 to about 60% by weight.
13. A glass enamel composition according to claim 8, wherein the glass frit component further contains one or more other low temperature melting glass frits.
14. A glass enamel composition according to claim 8, which further contains up to about 20% by weight solids of a crystalline seed material.
15. A glass enamel composition according to claim 14, wherein the crystalline seed material is bismuth silicate. -
16. A non-porous substrate having a glass enamel composition as defined in claim 8 fired thereon.
17. A substrate according to claim 16, which is automotive glass.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/908,953 | 1997-08-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
MXPA98006312A true MXPA98006312A (en) | 1999-06-01 |
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