CA1333813C - Glass enamel coating compositions - Google Patents
Glass enamel coating compositionsInfo
- Publication number
- CA1333813C CA1333813C CA000613308A CA613308A CA1333813C CA 1333813 C CA1333813 C CA 1333813C CA 000613308 A CA000613308 A CA 000613308A CA 613308 A CA613308 A CA 613308A CA 1333813 C CA1333813 C CA 1333813C
- Authority
- CA
- Canada
- Prior art keywords
- composition
- glass
- enamel
- frit
- vehicle
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000011521 glass Substances 0.000 title claims abstract description 69
- 239000000203 mixture Substances 0.000 title claims abstract description 49
- 239000002320 enamel (paints) Substances 0.000 title claims abstract description 11
- 239000000843 powder Substances 0.000 claims abstract description 29
- 229910052751 metal Inorganic materials 0.000 claims abstract description 14
- 239000002184 metal Substances 0.000 claims abstract description 14
- 239000000049 pigment Substances 0.000 claims abstract description 12
- 238000000034 method Methods 0.000 claims abstract description 11
- 150000004706 metal oxides Chemical class 0.000 claims abstract description 10
- 229910044991 metal oxide Inorganic materials 0.000 claims abstract description 9
- 230000006872 improvement Effects 0.000 claims abstract description 6
- 210000003298 dental enamel Anatomy 0.000 claims description 38
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 14
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 9
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 8
- 229910052718 tin Inorganic materials 0.000 claims description 8
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 7
- 229910052759 nickel Inorganic materials 0.000 claims description 7
- 229910052710 silicon Inorganic materials 0.000 claims description 7
- 239000010703 silicon Substances 0.000 claims description 7
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 6
- 229910052804 chromium Inorganic materials 0.000 claims description 6
- 239000011651 chromium Substances 0.000 claims description 6
- 229910017052 cobalt Inorganic materials 0.000 claims description 6
- 239000010941 cobalt Substances 0.000 claims description 6
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 6
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 6
- 229910052714 tellurium Inorganic materials 0.000 claims description 6
- 229910052719 titanium Inorganic materials 0.000 claims description 6
- 239000010936 titanium Substances 0.000 claims description 6
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 6
- 229910052721 tungsten Inorganic materials 0.000 claims description 6
- 239000010937 tungsten Substances 0.000 claims description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 5
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 5
- 229910052797 bismuth Inorganic materials 0.000 claims description 5
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims description 5
- 229910052802 copper Inorganic materials 0.000 claims description 5
- 239000010949 copper Substances 0.000 claims description 5
- 239000002245 particle Substances 0.000 claims description 5
- 239000010665 pine oil Substances 0.000 claims description 5
- 229910001220 stainless steel Inorganic materials 0.000 claims description 5
- 239000010935 stainless steel Substances 0.000 claims description 5
- 239000000758 substrate Substances 0.000 claims description 5
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 claims description 5
- 239000011135 tin Substances 0.000 claims description 5
- 229910052725 zinc Inorganic materials 0.000 claims description 5
- 239000011701 zinc Substances 0.000 claims description 5
- 229910052596 spinel Inorganic materials 0.000 claims description 4
- 239000011029 spinel Substances 0.000 claims description 4
- 229910003470 tongbaite Inorganic materials 0.000 claims description 3
- XFRVVPUIAFSTFO-UHFFFAOYSA-N 1-Tridecanol Chemical compound CCCCCCCCCCCCCO XFRVVPUIAFSTFO-UHFFFAOYSA-N 0.000 claims description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 2
- 229910052782 aluminium Inorganic materials 0.000 claims description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 2
- 229910052796 boron Inorganic materials 0.000 claims description 2
- 229910052791 calcium Inorganic materials 0.000 claims description 2
- 239000011575 calcium Substances 0.000 claims description 2
- 229910052744 lithium Inorganic materials 0.000 claims description 2
- 239000002480 mineral oil Substances 0.000 claims description 2
- 239000003208 petroleum Substances 0.000 claims description 2
- 239000011591 potassium Substances 0.000 claims description 2
- 229910052700 potassium Inorganic materials 0.000 claims description 2
- 229910052708 sodium Inorganic materials 0.000 claims description 2
- 239000011734 sodium Substances 0.000 claims description 2
- 229940087291 tridecyl alcohol Drugs 0.000 claims description 2
- 235000015112 vegetable and seed oil Nutrition 0.000 claims description 2
- 239000008158 vegetable oil Substances 0.000 claims description 2
- 229910052726 zirconium Inorganic materials 0.000 claims description 2
- UFGZSIPAQKLCGR-UHFFFAOYSA-N chromium carbide Chemical compound [Cr]#C[Cr]C#[Cr] UFGZSIPAQKLCGR-UHFFFAOYSA-N 0.000 claims 2
- 239000005388 borosilicate glass Substances 0.000 claims 1
- 239000002657 fibrous material Substances 0.000 claims 1
- 235000012245 magnesium oxide Nutrition 0.000 claims 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical class [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims 1
- 239000003039 volatile agent Substances 0.000 claims 1
- 238000000576 coating method Methods 0.000 abstract description 12
- 238000012423 maintenance Methods 0.000 abstract description 2
- 239000000463 material Substances 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 5
- 230000008901 benefit Effects 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 3
- 238000005299 abrasion Methods 0.000 description 3
- 239000000919 ceramic Substances 0.000 description 3
- 150000004673 fluoride salts Chemical class 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 238000007650 screen-printing Methods 0.000 description 3
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 230000004888 barrier function Effects 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 239000006105 batch ingredient Substances 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000011152 fibreglass Substances 0.000 description 2
- 238000007496 glass forming Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052748 manganese Inorganic materials 0.000 description 2
- 239000011572 manganese Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 230000005012 migration Effects 0.000 description 2
- 238000013508 migration Methods 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- -1 tellurium metals Chemical class 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- QHGNHLZPVBIIPX-UHFFFAOYSA-N tin(ii) oxide Chemical compound [Sn]=O QHGNHLZPVBIIPX-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 229910021418 black silicon Inorganic materials 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- GVEHJMMRQRRJPM-UHFFFAOYSA-N chromium(2+);methanidylidynechromium Chemical compound [Cr+2].[Cr]#[C-].[Cr]#[C-] GVEHJMMRQRRJPM-UHFFFAOYSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007607 die coating method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 229910021485 fumed silica Inorganic materials 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 239000000155 melt Substances 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
- 239000006060 molten glass Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 239000011819 refractory material Substances 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910000679 solder Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 238000005496 tempering Methods 0.000 description 1
- 239000005341 toughened glass Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
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
- C03C8/00—Enamels; Glazes; Fusion seal compositions being frit compositions having non-frit additions
- C03C8/14—Glass frit mixtures having non-frit additions, e.g. opacifiers, colorants, mill-additions
- C03C8/18—Glass frit mixtures having non-frit additions, e.g. opacifiers, colorants, mill-additions containing free metals
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B23/00—Re-forming shaped glass
- C03B23/02—Re-forming glass sheets
- C03B23/023—Re-forming glass sheets by bending
-
- 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
- C03C17/02—Surface treatment of glass, not in the form of fibres or filaments, by coating with glass
- C03C17/04—Surface treatment of glass, not in the form of fibres or filaments, by coating with glass by fritting glass powder
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Glass Compositions (AREA)
Abstract
In glass enamel coating compositions containing a glass frit system, optionally a metal oxide pigment and a vehicle therefor, the improvement comprising the presence therein of a series of metal powders to provide anti-stick, color maintenance and adhesion properties; the resulting coatings being particularly effective for application to glass sheets which are subsequently subjected to high temperature forming procedures.
Description
P-17247/=/CGC 1372 Glass ~namel Coating Com ositions Glass enamel paint compositions are well known to those skilled in the art. These materials can be utilized for a variety of applications but are of particul~r use in decorating glass sheets. For example, the coatings may be used to form borders around the edge of glass sheets which are converted into windshields, sidelites or backlites in motor vehicles.
It has been noted, however, that when glass sheets having the glass enamel coated thereon are subjected to a forming process at elevated temperatures, the prior art coatings exhibit a tendency to adhere to the materials covering the forming die. Accordingly, such prior art materials are unavailable for use in glass forming processes in which a heated glass sheet coated with the glass enamel is engaged by a material-covered forming die, generally a fiberglass-covered forming die.
Various aproaches have been suggested in order to facilitate the forming of glass sheets with a glass enamel coated thereon and to withstand the elevated bending or forming temperatures and the repeated contact of the glass sheet and the covered forming die without having the enamel adhere to the forming die. For example, U.S. 4,596,590 discloses the addition of metal oxide powder, including ferrous oxide, to the paint composition to provide the desired non-stick barrier between the coating and the fiberglass-covered forming die. U.S. 4,684,388 and U.S.
4,684,389 disclose similar approaches, the former patent adding a mixture of finely divided zinc metal powder and finely divided stannous oxide powder as the anti-stick barrier and the latter patent adding finely divided zinc metal powder for the similar effect. Although each of 1 33381 ~
It has been noted, however, that when glass sheets having the glass enamel coated thereon are subjected to a forming process at elevated temperatures, the prior art coatings exhibit a tendency to adhere to the materials covering the forming die. Accordingly, such prior art materials are unavailable for use in glass forming processes in which a heated glass sheet coated with the glass enamel is engaged by a material-covered forming die, generally a fiberglass-covered forming die.
Various aproaches have been suggested in order to facilitate the forming of glass sheets with a glass enamel coated thereon and to withstand the elevated bending or forming temperatures and the repeated contact of the glass sheet and the covered forming die without having the enamel adhere to the forming die. For example, U.S. 4,596,590 discloses the addition of metal oxide powder, including ferrous oxide, to the paint composition to provide the desired non-stick barrier between the coating and the fiberglass-covered forming die. U.S. 4,684,388 and U.S.
4,684,389 disclose similar approaches, the former patent adding a mixture of finely divided zinc metal powder and finely divided stannous oxide powder as the anti-stick barrier and the latter patent adding finely divided zinc metal powder for the similar effect. Although each of 1 33381 ~
these systems has been effective in reducing the indicated problem, greater reduction of adhesion and further improvement of surface appearance are still desired.
This invention seeks to provide an improved glass enamel coating composition.
The invention also seeks to provide such coatings which are readily available for application to glass sheets and which exhibit anti-stick properties during glass formation.
Various other advantages of this invention will become apparent from the following description thereof.
It has now been surprisingly discovered that by introducing a variety of finely divided powders into glass enamel compositions, the difficulties encountered with prior art formulations are substantially overcome. Thus, the resulting compositions can be readily applied to glass sheets and facilitate the formation of a smooth continuous coating which does not adhere to the fibreglass die coating when the heated coated glass is contacted with such materials. Accordingly, the bending or forming operations are not hindered by the above described sticking phenomenon. In addition, such enamel compositions exhibit increased opacity and increased glass adhesion. In particular, the presence of the powder in UV curable coatings substantially eliminates the potential for release of the enamel from the glass substrate.
The invention thus relates to the improved glass enamel composition and to the glass forming method utilizing such enamels. More specifically, the glass enamel compositions contain, as the primary ingredients, finely divided powder, glass frit and vehicle, with the optional presence of metal oxide pigment.
In particular, the applicable powders include chromium, chromium carbide, cobalt, copper, manganese, stainless steel, nickel, silicon, tin, titanium, tungsten and tellurium metals, with manganese, nickel, tungsten, tellurium, silicon, chrome and tin powders showing to particular advantage. It is preferred that the powder exhibit an average particle size of smaller than 325 mesh (0.03 mm) (U.S. Standard Sieve Series), the performance of the metal powder being improved by the finer particle sizes.
Any conventional soft glass frit or frit mixture can be utilized in the instant formulation. The frit will generally be ground to pass through 325 mesh screen (U.S. Standard Sieve size).
The primary purpose of the frit is to bond the pigmentary product to the glass surface. The frit may comprise any appropriate combination of metal oxides. Typical oxides may be selected from the oxides of zinc, lead, bismuth, silicon, titanium, zirconium, sodium, boron, lithium, potassium, calcium, aluminum, tin, magnesium, and the like. Correspondingly, various fluorides may appear in the frit. The batch composition which will provide the above noted oxides and fluorides may contain various salts, such as oxides, carbonates, sulfates, nitrates, fluorides and the like, of the above noted metals. The batch ingredients are selected in order to achieve predetermined frit properties. Lead, zinc alkali and bismuth alkali borosilicate frits are preferred for purposes of this invention.
This invention seeks to provide an improved glass enamel coating composition.
The invention also seeks to provide such coatings which are readily available for application to glass sheets and which exhibit anti-stick properties during glass formation.
Various other advantages of this invention will become apparent from the following description thereof.
It has now been surprisingly discovered that by introducing a variety of finely divided powders into glass enamel compositions, the difficulties encountered with prior art formulations are substantially overcome. Thus, the resulting compositions can be readily applied to glass sheets and facilitate the formation of a smooth continuous coating which does not adhere to the fibreglass die coating when the heated coated glass is contacted with such materials. Accordingly, the bending or forming operations are not hindered by the above described sticking phenomenon. In addition, such enamel compositions exhibit increased opacity and increased glass adhesion. In particular, the presence of the powder in UV curable coatings substantially eliminates the potential for release of the enamel from the glass substrate.
The invention thus relates to the improved glass enamel composition and to the glass forming method utilizing such enamels. More specifically, the glass enamel compositions contain, as the primary ingredients, finely divided powder, glass frit and vehicle, with the optional presence of metal oxide pigment.
In particular, the applicable powders include chromium, chromium carbide, cobalt, copper, manganese, stainless steel, nickel, silicon, tin, titanium, tungsten and tellurium metals, with manganese, nickel, tungsten, tellurium, silicon, chrome and tin powders showing to particular advantage. It is preferred that the powder exhibit an average particle size of smaller than 325 mesh (0.03 mm) (U.S. Standard Sieve Series), the performance of the metal powder being improved by the finer particle sizes.
Any conventional soft glass frit or frit mixture can be utilized in the instant formulation. The frit will generally be ground to pass through 325 mesh screen (U.S. Standard Sieve size).
The primary purpose of the frit is to bond the pigmentary product to the glass surface. The frit may comprise any appropriate combination of metal oxides. Typical oxides may be selected from the oxides of zinc, lead, bismuth, silicon, titanium, zirconium, sodium, boron, lithium, potassium, calcium, aluminum, tin, magnesium, and the like. Correspondingly, various fluorides may appear in the frit. The batch composition which will provide the above noted oxides and fluorides may contain various salts, such as oxides, carbonates, sulfates, nitrates, fluorides and the like, of the above noted metals. The batch ingredients are selected in order to achieve predetermined frit properties. Lead, zinc alkali and bismuth alkali borosilicate frits are preferred for purposes of this invention.
The frit is prepared by melting the batch ingredients at temperatures of from about 900 to 1600C. and then quenching the molten glass either with the use of water or by pouring the melt between two cooled metal rolls rotating in opposite direction.
Melting generally is conducted in a ceramic or platinum crucible or in an appropriately lined furnace. The resulting chips, chunks or flakes of frit are then ground into fine particles.
The vehicle is selected on the basis of the end use application. It is essential that the vehicle adequately suspend the particulates and burn off completely upon firing of the composition. Vehicles are typically organic and include compositions based on pine oils, vegetable oils, mineral oils, low molecular weight petroleum fractions, tridecyl alcohol, and the like. The vehicles may be modified by viscous resins such as vinyl resins, solvents, film formers such as cellulosic materials, and the like.
Correspondingly, UV-base vehicles are equally applicable for use in the instant invention. Such UV-base vehicles are well known to those skilled in the art and will generally be 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. 4,306,012 and U.S. 4,649,062. As is recognized, such systems are cured with ultraviolet radiatlon after application to the glass substrate.
The modified glass enamels contain from about 2-75%
of powder and preferably 5-35%; from about 10 to 85%
B
Melting generally is conducted in a ceramic or platinum crucible or in an appropriately lined furnace. The resulting chips, chunks or flakes of frit are then ground into fine particles.
The vehicle is selected on the basis of the end use application. It is essential that the vehicle adequately suspend the particulates and burn off completely upon firing of the composition. Vehicles are typically organic and include compositions based on pine oils, vegetable oils, mineral oils, low molecular weight petroleum fractions, tridecyl alcohol, and the like. The vehicles may be modified by viscous resins such as vinyl resins, solvents, film formers such as cellulosic materials, and the like.
Correspondingly, UV-base vehicles are equally applicable for use in the instant invention. Such UV-base vehicles are well known to those skilled in the art and will generally be 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. 4,306,012 and U.S. 4,649,062. As is recognized, such systems are cured with ultraviolet radiatlon after application to the glass substrate.
The modified glass enamels contain from about 2-75%
of powder and preferably 5-35%; from about 10 to 85%
B
glass frit and preferably 30 to 65%; and from about 10 to 45% vehicle and preferably 14 to 30%. The percentages are based on the weight of the formulated glass enamel paste.
The resulting compositions will be viscous in na~ure, the viscosity depending on application method and end use. For purposes of screen printing, viscosities ranging from 10,000-80,000, and preferably 20,000-65,000, centipoises at 20C. as determined on a Brookfield Viscometer, ~7 spindle at 20 rpm are appropriate.
The optional metal oxide pigments are well known to those skilled in the art. Applicable oxides include, for example, chrome, cobalt, iron, nickel, copper, manganese, and the like. Although the latter metal oxides form preferred black spinel pigments, other metal oxides to produce different pigments and other colors are likewise contemplated. The pigment component will generally comprise from 10 to 40%, by weight, of the indicated glass frit.
A wide variety of other optional ingredients may be included in these formulations. These may be added to modify viscosity and to enhance properties such as bond strength and abrasion resistance. Various bismuth and bismuth-containing compounds for bond strength; certain refractory materials such as zirconium oxide to increase abrasion resistance; suspending agents such as iso-stearic acid; and fumed silica and other silica products to modify viscosity; may be included for the indicated benefits.
The compositions are prepared by blending the solid materials, adding the liquid ingredients thereto and then thoroughly mixing or kneading the two in order to form a smooth, thick paste. The paste is then further dispersed by means of a conventional machine such as a three-roll mill or dispersator such as a Cowles or Morehouse mill.
Methods for applying the enamel coatings are well known to those skilled in the art. The dispersed compositions may be applied by techniques such as screen printing, decal application, spraying, brushing, roller coating, and the like. Screen printing is preferred for purposes of applying the composition to glass substrates.
After the enamel has been applied to the glass sheet, the glass sheet is heated to a temperature which softens the glass sufficiently so that the glass sheet can be formed. Generally, this temperature is in a range of about 600-760C. Compositions which are formulated to be responsive to UV radiation may be exposed to such radiation prior to heating to bond the enamel to the glass sheet.
After heating, the glass sheet and the enamel thereon are engaged by the fiberglass covered forming die to place the heated glass sheet into a desired shape. The heating operation, of course, burns off the organic materials contained in the enamel and bonds the remaining portion of the enamel to the glass sheet. The powder addition to the enamel serves to prevent sticking of any of the enamel to the forming die and also provides a smooth continuous surface to the resulting enamelled surface.
.
After the forming die has been removed from engagement with the glass sheet and the enamel without any sticking of the enamel thereto, the glass sheet may be cooled to obtain a formed glass sheet with enamel thereon.
3 33~$11 3 The glass sheet may be rapidly cooled in a glass tempering operation to achieve a tempered-glass product having the enamel thereon or annealed when utilized for windshield applications. The resulting glass sheet is then readily available for use in a variety of applications, particularly the automotive applications noted hereinabove.
Glass enamel paint compositions are also formulated with silver metal in order to provide conductive coatings for use, for example, as defrost circuits for automotive backlites and windshield. In such areas of utility, color maintenance, bond strength, solderability, absence of silver migration and abrasion resistance are required performance characteristics. It is to be noted that the instant metal powder-containing systems are applicable for use in conjunction with such conductive coatings for the above noted areas of utility. When the conductive coatings are applied in overlapping relationship with the metal powder-containing systems, performance improvements as observed after heat treatment include good resistance to silver migration into the enamel, substantial reduction of undesirable blue haze of the buss bar (bar connecting ends of individual horizontal conductive elements of defrost circuit) and permanence of solder connections.
The following examples further illustrate the embodiments of this invention. In these examples, all parts are given by weight unless otherwise specified.
- _ 1 3338 1 3 Example 1 This example illustrates the preparation and application of typical enamels of this invention.
The following formulation is prepared for each indicated metal powder.
parts Glass enamel powder * 3.6 Pine Oil-based vehicle 1.35 Metal powder 1.4 * 58 parts lead-alumina-borosilicate frit 42 parts black spinel pigment blend The enamels are prepared by blending the liquid and solid ingredients and then dispersing the paste in an appropriate mill.
The performance characteristics of the enamels are determined in a laboratory screening procedure by applying the enamels to microscope slides, heating the slide to 705C
for 15 minutes, impressing a slightly curved, ceramic cloth covered press bar at a estimated pressure of 25-50 pounds onto the softened glass for a period of five seconds with a rolling motion, removing the press bar and visually iden-tifying the degree of adhesion between the enamel and the ceramic cloth. A rating of "O" is indicative of the absence of adherance; "1" indicates slight adherance; "2" indicates modest-noticeable adherance; and "3" indicates significant adherance.
In addition, the color and absence of porosity of the enamel coating are visually determined by inspecting the ~ 33~ 3 slide through the uncoated ~underneath) side. The surface appearance of the coating is also visually determined.
The results are tabulated below:
Metal Rating Color PorositY APpearance Manganese 0-1 black exc. matte gray/black Chromium 2-3 black exc. black-sl. gloss (325 mesh) Cobalt 2-3 black exc. black-sl. gloss Copper 1 redtbrown exc. matte gray Nickel 1-2 black exc. matte gray~black Tellurium 0smokey brown fair smooth gray/black Tin 1 gray/black exc. matte gray~black Titanium 1-2 black exc. rough-matte black Tungsten 1 black exc. matte gray/black These data thus indicate the performance benefits of the enamels of this invention.
ExamPle 2 The preparative and test procedures of Example 1 are repeated with the exception that the indicated powders are further finely ground to varying degrees to achieve finer particle size (below about 0.03 mm) and increased surface area.
Powder Ratinq Color PorositY APPearance Cobalt 1 black exc. matte black Chromium 1 weak black exc. matte-sl.gloss black carbide Chromium 0 black exc. matte black Silicon 0 gray/black exc. matte black Manganese 0 black exc. matte gray/black ExamPle 3 The preparative and test procedures of Example 1 are again repeated.
Metal Averaqe Particle Size (u) Ratinq Stainless steel 12.36 2 Summarizing, this invention provides glass enamel compositions exhibiting a wide variety of performance improvements a~ a result of the presence of various finely divided powders therein. Variations may be made in procedures, proportions and materials without departing from the scope of the invention as defined by the following claims.
The resulting compositions will be viscous in na~ure, the viscosity depending on application method and end use. For purposes of screen printing, viscosities ranging from 10,000-80,000, and preferably 20,000-65,000, centipoises at 20C. as determined on a Brookfield Viscometer, ~7 spindle at 20 rpm are appropriate.
The optional metal oxide pigments are well known to those skilled in the art. Applicable oxides include, for example, chrome, cobalt, iron, nickel, copper, manganese, and the like. Although the latter metal oxides form preferred black spinel pigments, other metal oxides to produce different pigments and other colors are likewise contemplated. The pigment component will generally comprise from 10 to 40%, by weight, of the indicated glass frit.
A wide variety of other optional ingredients may be included in these formulations. These may be added to modify viscosity and to enhance properties such as bond strength and abrasion resistance. Various bismuth and bismuth-containing compounds for bond strength; certain refractory materials such as zirconium oxide to increase abrasion resistance; suspending agents such as iso-stearic acid; and fumed silica and other silica products to modify viscosity; may be included for the indicated benefits.
The compositions are prepared by blending the solid materials, adding the liquid ingredients thereto and then thoroughly mixing or kneading the two in order to form a smooth, thick paste. The paste is then further dispersed by means of a conventional machine such as a three-roll mill or dispersator such as a Cowles or Morehouse mill.
Methods for applying the enamel coatings are well known to those skilled in the art. The dispersed compositions may be applied by techniques such as screen printing, decal application, spraying, brushing, roller coating, and the like. Screen printing is preferred for purposes of applying the composition to glass substrates.
After the enamel has been applied to the glass sheet, the glass sheet is heated to a temperature which softens the glass sufficiently so that the glass sheet can be formed. Generally, this temperature is in a range of about 600-760C. Compositions which are formulated to be responsive to UV radiation may be exposed to such radiation prior to heating to bond the enamel to the glass sheet.
After heating, the glass sheet and the enamel thereon are engaged by the fiberglass covered forming die to place the heated glass sheet into a desired shape. The heating operation, of course, burns off the organic materials contained in the enamel and bonds the remaining portion of the enamel to the glass sheet. The powder addition to the enamel serves to prevent sticking of any of the enamel to the forming die and also provides a smooth continuous surface to the resulting enamelled surface.
.
After the forming die has been removed from engagement with the glass sheet and the enamel without any sticking of the enamel thereto, the glass sheet may be cooled to obtain a formed glass sheet with enamel thereon.
3 33~$11 3 The glass sheet may be rapidly cooled in a glass tempering operation to achieve a tempered-glass product having the enamel thereon or annealed when utilized for windshield applications. The resulting glass sheet is then readily available for use in a variety of applications, particularly the automotive applications noted hereinabove.
Glass enamel paint compositions are also formulated with silver metal in order to provide conductive coatings for use, for example, as defrost circuits for automotive backlites and windshield. In such areas of utility, color maintenance, bond strength, solderability, absence of silver migration and abrasion resistance are required performance characteristics. It is to be noted that the instant metal powder-containing systems are applicable for use in conjunction with such conductive coatings for the above noted areas of utility. When the conductive coatings are applied in overlapping relationship with the metal powder-containing systems, performance improvements as observed after heat treatment include good resistance to silver migration into the enamel, substantial reduction of undesirable blue haze of the buss bar (bar connecting ends of individual horizontal conductive elements of defrost circuit) and permanence of solder connections.
The following examples further illustrate the embodiments of this invention. In these examples, all parts are given by weight unless otherwise specified.
- _ 1 3338 1 3 Example 1 This example illustrates the preparation and application of typical enamels of this invention.
The following formulation is prepared for each indicated metal powder.
parts Glass enamel powder * 3.6 Pine Oil-based vehicle 1.35 Metal powder 1.4 * 58 parts lead-alumina-borosilicate frit 42 parts black spinel pigment blend The enamels are prepared by blending the liquid and solid ingredients and then dispersing the paste in an appropriate mill.
The performance characteristics of the enamels are determined in a laboratory screening procedure by applying the enamels to microscope slides, heating the slide to 705C
for 15 minutes, impressing a slightly curved, ceramic cloth covered press bar at a estimated pressure of 25-50 pounds onto the softened glass for a period of five seconds with a rolling motion, removing the press bar and visually iden-tifying the degree of adhesion between the enamel and the ceramic cloth. A rating of "O" is indicative of the absence of adherance; "1" indicates slight adherance; "2" indicates modest-noticeable adherance; and "3" indicates significant adherance.
In addition, the color and absence of porosity of the enamel coating are visually determined by inspecting the ~ 33~ 3 slide through the uncoated ~underneath) side. The surface appearance of the coating is also visually determined.
The results are tabulated below:
Metal Rating Color PorositY APpearance Manganese 0-1 black exc. matte gray/black Chromium 2-3 black exc. black-sl. gloss (325 mesh) Cobalt 2-3 black exc. black-sl. gloss Copper 1 redtbrown exc. matte gray Nickel 1-2 black exc. matte gray~black Tellurium 0smokey brown fair smooth gray/black Tin 1 gray/black exc. matte gray~black Titanium 1-2 black exc. rough-matte black Tungsten 1 black exc. matte gray/black These data thus indicate the performance benefits of the enamels of this invention.
ExamPle 2 The preparative and test procedures of Example 1 are repeated with the exception that the indicated powders are further finely ground to varying degrees to achieve finer particle size (below about 0.03 mm) and increased surface area.
Powder Ratinq Color PorositY APPearance Cobalt 1 black exc. matte black Chromium 1 weak black exc. matte-sl.gloss black carbide Chromium 0 black exc. matte black Silicon 0 gray/black exc. matte black Manganese 0 black exc. matte gray/black ExamPle 3 The preparative and test procedures of Example 1 are again repeated.
Metal Averaqe Particle Size (u) Ratinq Stainless steel 12.36 2 Summarizing, this invention provides glass enamel compositions exhibiting a wide variety of performance improvements a~ a result of the presence of various finely divided powders therein. Variations may be made in procedures, proportions and materials without departing from the scope of the invention as defined by the following claims.
Claims (17)
1. In a glass enamel coating composition comprising a glass frit composition, and a vehicle therefor, the improvement comprising the presence therein of 2-75%, by weight, of a finely divided powder selected from the group consisting of chromium, chromium carbide, cobalt, copper, manganese, stainless steel, nickel, silicon, tin, titanium, tungsten and tellurium powders, and mixtures thereof.
2. The composition of claim 1, wherein said powder is selected from the group consisting of manganese, nickel, tungsten, tellurium, silicon, chrome, tin and stainless steel.
3. The composition of claim 1, wherein the average particle size of the powder is less than about 0.03 mm.
4. The composition of claim 1, wherein said glass frit comprises a combination of metal oxides.
5. The composition of claim 4, wherein said oxides are selected from the group consisting of zinc, lead, bismuth, silicon, titanium, zirconium, sodium, boron, lithium, potassium, calcium, aluminum, tin and magnesium oxides.
11a
11a
6. The composition of claim 5, wherein said frit is a lead borosilicate glass frit.
7. The composition of claim 1, wherein an organic vehicle is present.
8. The composition of claim 7, wherein said vehicle is based on pine oil, vegetable oils, mineral oils, low molecular weight petroleum fractions or tridecyl alcohol.
9. The composition of claim 8, wherein said vehicle is based on pine oil.
10. The composition of claim 1 which also contains a metal oxide pigment.
11. The composition of claim 10, wherein said pigment is a black spinel pigment.
12. The composition of claim 10, which comprises a lead-borosilicate frit, a black spinel pigment, a finely divided metal powder and a pine oil-based vehicle therefor.
13. The composition of claim 1, wherein said vehicle is UV-curable.
14. A glass substrate coated on sections thereof with a glass enamel coating composition of claim 1.
15. A glass substrate coated on sections thereof with a glass enamel coating composition of claim 10.
16. In the method for forming a glass enamel coated glass sheet, the glass enamel composition comprising a glass frit system and a vehicle therefor, wherein the glass enamel composition is coated onto the glass sheet, the coated glass sheet is heated to soften the sheet, to remove the volatiles in said enamel and to bond the remainder of the enamel to the sheet, the softened glass sheet is contacted with a fibrous material covered forming die, the forming die is removed and the glass sheet is cooled; the improvement comprising incorporating into the enamel composition from about 2-75%, by weight, of a finely divided powder selected from the group consisting of chromium, chromium carbide, cobalt, copper, manganese, stainless steel, nickel, silicon, tin, titanium, tungsten and tellurium powders and mixtures thereof.
17. The method of claim 16, wherein said glass enamel coating composition also contains a metal oxide pigment.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US25046088A | 1988-09-28 | 1988-09-28 | |
US250,460 | 1988-09-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1333813C true CA1333813C (en) | 1995-01-03 |
Family
ID=22947844
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA000613308A Expired - Lifetime CA1333813C (en) | 1988-09-28 | 1989-09-26 | Glass enamel coating compositions |
Country Status (8)
Country | Link |
---|---|
EP (1) | EP0362136B1 (en) |
JP (1) | JPH02129043A (en) |
KR (1) | KR0131588B1 (en) |
BR (1) | BR8904897A (en) |
CA (1) | CA1333813C (en) |
DE (1) | DE58906485D1 (en) |
ES (1) | ES2047706T3 (en) |
MX (1) | MX169537B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7695556B2 (en) * | 2006-08-30 | 2010-04-13 | Corning Incorporated | Ink for printing data carrying mark on honeycomb structures |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE69115372T2 (en) * | 1990-07-12 | 1996-05-09 | Ford Werke Ag | Composition of ceramic glaze |
WO1992003356A1 (en) * | 1990-08-13 | 1992-03-05 | Kohjin Co., Ltd. | Food packaging bag |
CA2052866A1 (en) * | 1990-12-10 | 1992-06-11 | Premakaran T. Boaz | Process for manufacturing a formed glass sheet having paint thereon |
EP0510542A1 (en) * | 1991-04-24 | 1992-10-28 | Asahi Glass Company Ltd. | Ceramic color composition and process for producing a sheet glass employing it |
JPH07507536A (en) * | 1993-03-26 | 1995-08-24 | サン−ゴバン ビトラージュ | Method for producing glazed laminated window glass and glaze composition used therefor |
FR2705335B1 (en) * | 1993-05-13 | 1995-07-21 | Saint Gobain Vitrage Int | Composition for the enamelling of glass substrates, application to laminated glazing and products obtained. |
FR2703043B1 (en) * | 1993-03-26 | 1995-10-20 | Saint Gobain Vitrage Int | Composition for glazing glass substrates, application to laminated glazing and products obtained. |
FR2724377B1 (en) | 1994-09-09 | 1996-10-31 | Saint Gobain Vitrage | EMAIL COMPOSITION FOR GLASS SUBSTRATE |
FR2728558A1 (en) | 1994-12-23 | 1996-06-28 | Saint Gobain Vitrage | METHOD FOR ENAMELLING GLASS SUBSTRATES AND COMPOSITION USED THEREFOR |
DE19502653A1 (en) * | 1995-01-28 | 1996-08-01 | Cerdec Ag | Lead-free glass composition and its use |
KR100442921B1 (en) * | 2001-10-26 | 2004-08-02 | 주식회사 엘지화학 | Graft copolymer resin of vinyl chloride having superior heat resistance and anti-stress impact and method for preparing thereof |
KR100478583B1 (en) * | 2001-11-16 | 2005-03-28 | 주식회사 서울세라믹스 | Glaze composition for metallic tile using thereof and Preparing method |
ITFI20050142A1 (en) * | 2005-06-23 | 2006-12-24 | Colorobbia Italiana Spa | MATERIALS FOR THE COVERING OF CERAMIC BODIES, PROCESSED FOR THEIR PREPARATION THEIR USE AND THE CERAMIC ARTICLES THAT INCLUDE THEM |
KR100781335B1 (en) * | 2006-07-13 | 2007-11-30 | 한국전력공사 | Method for Improving Hardness and Erosion Resistance of Glass Enamel Coating Layer of Carbon Steel |
ES2310139B1 (en) * | 2007-06-12 | 2009-12-04 | Consejo Superior De Investigaciones Cientificas | CERAMIC ENAMEL WITH METAL GLOSS, PROCEDURE OF OBTAINING AND APPLICATION. |
US8952245B2 (en) * | 2012-01-23 | 2015-02-10 | Heraeus Precious Metals North America Conshohocken Llc | Conductive thick film paste for solar cell contacts |
DE102013108428A1 (en) | 2013-08-05 | 2015-02-05 | Tenedora Nemak, S.A. De C.V. | Enamel powder, metal component with a surface portion provided with an enamel coating and method for producing such a metal component |
FR3118026B1 (en) | 2020-12-22 | 2023-08-18 | Saint Gobain | Motor vehicle roof glazing |
CN112624581B (en) * | 2020-12-23 | 2022-12-16 | 安徽金龙浩光电科技有限公司 | 3D glass hot bending process |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3060559D1 (en) * | 1979-01-17 | 1982-08-12 | Bayer Ag | Coated metal article and method of manufacturing it |
US4306012A (en) * | 1979-12-05 | 1981-12-15 | Hercules Incorporated | Process of radiation and heat treatment of printing medium |
US4649062A (en) * | 1983-01-05 | 1987-03-10 | Ciba-Geigy Corporation | Ultraviolet radiation curable vehicle for ceramic colors, composition and method |
DE3503929A1 (en) * | 1985-02-06 | 1986-08-07 | Reimbold & Strick GmbH & Co, 5000 Köln | CERAMIC COMPOSITIONS AND THEIR USE |
US4596590A (en) * | 1985-04-29 | 1986-06-24 | Ford Motor Company | Method of forming a glass sheet with a ceramic paint thereon |
US4684388A (en) * | 1986-12-01 | 1987-08-04 | Ford Motor Company | Method of forming a glass sheet with a UV-base ceramic paint thereon |
US4684389A (en) * | 1986-12-01 | 1987-08-04 | Ford Motor Company | Method of forming a glass sheet with an oil-base ceramic paint thereon |
DE58902785D1 (en) * | 1988-01-29 | 1993-01-07 | Ciba Geigy Ag | ENAMEL COMPOSITIONS FOR COATINGS. |
-
1989
- 1989-09-19 EP EP89810709A patent/EP0362136B1/en not_active Expired - Lifetime
- 1989-09-19 DE DE89810709T patent/DE58906485D1/en not_active Expired - Fee Related
- 1989-09-19 ES ES89810709T patent/ES2047706T3/en not_active Expired - Lifetime
- 1989-09-26 MX MX017692A patent/MX169537B/en unknown
- 1989-09-26 CA CA000613308A patent/CA1333813C/en not_active Expired - Lifetime
- 1989-09-26 KR KR89013818A patent/KR0131588B1/en not_active IP Right Cessation
- 1989-09-27 BR BR898904897A patent/BR8904897A/en not_active IP Right Cessation
- 1989-09-28 JP JP1250829A patent/JPH02129043A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7695556B2 (en) * | 2006-08-30 | 2010-04-13 | Corning Incorporated | Ink for printing data carrying mark on honeycomb structures |
Also Published As
Publication number | Publication date |
---|---|
DE58906485D1 (en) | 1994-02-03 |
BR8904897A (en) | 1990-05-08 |
KR0131588B1 (en) | 1998-04-09 |
ES2047706T3 (en) | 1994-03-01 |
MX169537B (en) | 1993-07-09 |
EP0362136A2 (en) | 1990-04-04 |
EP0362136B1 (en) | 1993-12-22 |
KR900004876A (en) | 1990-04-13 |
JPH02129043A (en) | 1990-05-17 |
EP0362136A3 (en) | 1990-10-17 |
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