WO1996041773A1 - Pate d'impression apte a la cuisson pour imprimer des surfaces de verre et procede pour fabriquer ladite pate - Google Patents
Pate d'impression apte a la cuisson pour imprimer des surfaces de verre et procede pour fabriquer ladite pate Download PDFInfo
- Publication number
- WO1996041773A1 WO1996041773A1 PCT/FR1996/000819 FR9600819W WO9641773A1 WO 1996041773 A1 WO1996041773 A1 WO 1996041773A1 FR 9600819 W FR9600819 W FR 9600819W WO 9641773 A1 WO9641773 A1 WO 9641773A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- glass
- pigments
- printing paste
- gel
- composition
- Prior art date
Links
- 239000011521 glass Substances 0.000 title claims abstract description 102
- 238000007639 printing Methods 0.000 title claims abstract description 65
- 238000000034 method Methods 0.000 title claims description 12
- 239000000049 pigment Substances 0.000 claims abstract description 76
- 239000000203 mixture Substances 0.000 claims abstract description 55
- 239000011230 binding agent Substances 0.000 claims abstract description 11
- 238000003980 solgel method Methods 0.000 claims abstract description 3
- 238000000576 coating method Methods 0.000 claims description 39
- 239000011248 coating agent Substances 0.000 claims description 30
- 238000002844 melting Methods 0.000 claims description 28
- 230000008018 melting Effects 0.000 claims description 27
- 239000000843 powder Substances 0.000 claims description 23
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 claims description 15
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 14
- 238000010411 cooking Methods 0.000 claims description 13
- 238000010438 heat treatment Methods 0.000 claims description 11
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 9
- 239000006060 molten glass Substances 0.000 claims description 8
- 239000012298 atmosphere Substances 0.000 claims description 5
- 229910002804 graphite Inorganic materials 0.000 claims description 5
- 239000010439 graphite Substances 0.000 claims description 5
- 239000000758 substrate Substances 0.000 claims description 5
- 229910020617 PbO—B2O3—SiO2 Inorganic materials 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 230000001681 protective effect Effects 0.000 claims description 4
- 229910052782 aluminium Inorganic materials 0.000 claims description 3
- 229910052791 calcium Inorganic materials 0.000 claims description 3
- 239000000470 constituent Substances 0.000 claims description 3
- LIKBJVNGSGBSGK-UHFFFAOYSA-N iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Fe+3].[Fe+3] LIKBJVNGSGBSGK-UHFFFAOYSA-N 0.000 claims description 3
- 229910052726 zirconium Inorganic materials 0.000 claims description 3
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 claims description 2
- 229910052797 bismuth Inorganic materials 0.000 claims description 2
- 229910052796 boron Inorganic materials 0.000 claims description 2
- 239000006229 carbon black Substances 0.000 claims description 2
- 230000008859 change Effects 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 229910052595 hematite Inorganic materials 0.000 claims description 2
- 239000011019 hematite Substances 0.000 claims description 2
- 229910052749 magnesium Inorganic materials 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 229910052698 phosphorus Inorganic materials 0.000 claims description 2
- 229910052708 sodium Inorganic materials 0.000 claims description 2
- 229910052719 titanium Inorganic materials 0.000 claims description 2
- 239000010936 titanium Substances 0.000 claims description 2
- 230000009466 transformation Effects 0.000 claims description 2
- 229910052725 zinc Inorganic materials 0.000 claims description 2
- 239000000463 material Substances 0.000 claims 3
- 238000006243 chemical reaction Methods 0.000 claims 1
- 238000007496 glass forming Methods 0.000 claims 1
- 230000009931 harmful effect Effects 0.000 claims 1
- 238000001035 drying Methods 0.000 abstract description 3
- 239000001023 inorganic pigment Substances 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 12
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 12
- 210000003298 dental enamel Anatomy 0.000 description 11
- WRECIMRULFAWHA-UHFFFAOYSA-N trimethyl borate Chemical compound COB(OC)OC WRECIMRULFAWHA-UHFFFAOYSA-N 0.000 description 10
- QQQSFSZALRVCSZ-UHFFFAOYSA-N triethoxysilane Chemical compound CCO[SiH](OCC)OCC QQQSFSZALRVCSZ-UHFFFAOYSA-N 0.000 description 8
- 239000005329 float glass Substances 0.000 description 7
- 230000008569 process Effects 0.000 description 7
- 239000002689 soil Substances 0.000 description 7
- 238000001694 spray drying Methods 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 5
- 238000007650 screen-printing Methods 0.000 description 5
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 229910052500 inorganic mineral Inorganic materials 0.000 description 4
- 239000011707 mineral Substances 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- RLJMLMKIBZAXJO-UHFFFAOYSA-N lead nitrate Chemical compound [O-][N+](=O)O[Pb]O[N+]([O-])=O RLJMLMKIBZAXJO-UHFFFAOYSA-N 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 238000004064 recycling Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- 239000005388 borosilicate glass Substances 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- JGDFBJMWFLXCLJ-UHFFFAOYSA-N copper chromite Chemical compound [Cu]=O.[Cu]=O.O=[Cr]O[Cr]=O JGDFBJMWFLXCLJ-UHFFFAOYSA-N 0.000 description 2
- 239000006063 cullet Substances 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 238000000265 homogenisation Methods 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 239000000976 ink Substances 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 229910017604 nitric acid Inorganic materials 0.000 description 2
- 239000012299 nitrogen atmosphere Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000011253 protective coating Substances 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 229910052596 spinel Inorganic materials 0.000 description 2
- 239000011029 spinel Substances 0.000 description 2
- 229910052566 spinel group Inorganic materials 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 241000779819 Syncarpia glomulifera Species 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 230000035508 accumulation Effects 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- QXJJQWWVWRCVQT-UHFFFAOYSA-K calcium;sodium;phosphate Chemical compound [Na+].[Ca+2].[O-]P([O-])([O-])=O QXJJQWWVWRCVQT-UHFFFAOYSA-K 0.000 description 1
- SXKJCXWNWBRZGB-UHFFFAOYSA-N chromium copper manganese Chemical compound [Mn][Cr][Cu] SXKJCXWNWBRZGB-UHFFFAOYSA-N 0.000 description 1
- 230000001427 coherent effect Effects 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000000280 densification Methods 0.000 description 1
- 238000004455 differential thermal analysis Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000010981 drying operation Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- 235000013980 iron oxide Nutrition 0.000 description 1
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 210000003739 neck Anatomy 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000001739 pinus spp. Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000004901 spalling Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 229940036248 turpentine Drugs 0.000 description 1
- 238000002604 ultrasonography Methods 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- YZYKBQUWMPUVEN-UHFFFAOYSA-N zafuleptine Chemical compound OC(=O)CCCCCC(C(C)C)NCC1=CC=C(F)C=C1 YZYKBQUWMPUVEN-UHFFFAOYSA-N 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/03—Printing inks characterised by features other than the chemical nature of the binder
- C09D11/037—Printing inks characterised by features other than the chemical nature of the binder characterised by the pigment
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M1/00—Inking and printing with a printer's forme
- B41M1/26—Printing on other surfaces than ordinary paper
- B41M1/34—Printing on other surfaces than ordinary paper on glass or ceramic surfaces
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/28—Compounds of silicon
- C09C1/30—Silicic acid
- C09C1/3045—Treatment with inorganic compounds
- C09C1/3054—Coating
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/36—Compounds of titanium
- C09C1/3607—Titanium dioxide
- C09C1/3653—Treatment with inorganic compounds
- C09C1/3661—Coating
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/44—Carbon
- C09C1/48—Carbon black
- C09C1/56—Treatment of carbon black ; Purification
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/62—Metallic pigments or fillers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C3/00—Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
- C09C3/06—Treatment with inorganic compounds
- C09C3/063—Coating
Definitions
- the present invention relates to a baking printing paste for printing glass surfaces, comprising at least one glass composition (for example a glass frit), one or more inorganic colored pigments and an organic and / or inorganic binder to impart the flow properties necessary for the printing operation and to achieve sufficient mechanical strength of the printed layer after drying.
- the invention also relates to a process for the preparation of such a printing paste.
- Enamel-type baking inks are often applied for decorative purposes or for technical reasons on glass bodies, for example on glass sheets, and are fired at high temperatures.
- This technique is applied on a large scale for automotive glazing when the glazing is mounted, using the bonding technique, in the window frames of the bodywork.
- a frame-shaped layer made of an opaque baking ink for visible light and UV radiation is usually applied by screen printing on the glazing.
- the applied layer after an operation of drying, is cooked during a subsequent bending and / or quenching operation.
- the purpose of the baked enamel layer is to prevent the adhesive region from being seen from the outside through the glazing and also to protect the adhesive from UV rays which can lead to spalling of the adhesive. over time.
- the printing pastes known for the preparation of such enamel-type layers contain as color pigments minerals with high melting point, for example copper-chromium-manganese spinel (CuO-Cr 2 O 3 -MnO) for the black color, mixtures of this spinel with titanium dioxide (TiO 2 ) for the gray color, or mixtures of spinels formed by Sn, V, Fe, Zr, Si, Co, Al, Ni and Ca for others desired colors.
- CuO-Cr 2 O 3 -MnO copper-chromium-manganese spinel
- TiO 2 titanium dioxide
- spinels formed by Sn, V, Fe, Zr, Si, Co, Al, Ni and Ca for others desired colors.
- Known printing pastes also include a glass frit which is present in the printing paste, like pigments, in the form of a finely ground powder and which, during the cooking operation (carried out, by example, at a temperature between 500 and 750-800 ° C) melts by partially or completely coating the colored pigments, so that after cooling, an enamel-like layer is firmly united on the surface of the glass substrate.
- a glass frit which is present in the printing paste, like pigments, in the form of a finely ground powder and which, during the cooking operation (carried out, by example, at a temperature between 500 and 750-800 ° C) melts by partially or completely coating the colored pigments, so that after cooling, an enamel-like layer is firmly united on the surface of the glass substrate.
- thermally and chemically stable inorganic materials or substances are used as colored pigments, that is to say only substances which do not thermally decompose at cooking temperature or chemically react with d 'other constituents of the printing paste or with the ambient atmosphere and therefore do not change their color or other properties.
- magnetite (Fe 3 O) cannot so far be used as a colored pigment, because at the firing temperature it oxidizes to hematite (Fe 2 O 3 ) which as such no longer has the properties of desired coloring.
- the recycling of printed glazings by adding to the vitrifiable mixture of cullet provided with these known enamel layers during the melting of the glass frequently gives rise to difficulties.
- the colored pigments remain contained as such in the molten glass.
- other colored pigments which s distribute as dissolved oxides in the molten glass it can also happen that they undesirably influence the properties of the glass, by modifying, for example, the viscosity of the molten glass, the color of the glazing obtained and / or other physical properties of molten glass and / or glazing. For this reason, it has hitherto not been possible to recycle glazing which is provided with a layer of baked enamel of known compositions, for example for the manufacture of high optical quality float glass.
- the object of the invention is to prepare, for printing glass surfaces, baking printing pastes having a greater field of application and which can use a greater variety of components, in particular as regards the possibility of using less stable colored pigments.
- the invention resides in the fact that the pigments present in the dough ready for printing and baking are coated as such with a layer of a glass or a gel (or xerogel) with a suitable vitrifiable composition thermally solidified.
- the printing paste suitable for cooking according to the present invention thus comprises at least one glass composition, one or more pigments and an organic and / or inorganic binder, the pigments being coated as such with a layer of a glass or a gel of a thermally solidified vitrifiable composition.
- the pigments, present in the uncooked dough are coated with a layer with a thickness of 0.5 to 5 ⁇ m of a glass or a gel of a thermally solidified vitrifiable composition.
- composition is meant by extension, one or more components.
- glass composition is meant a vitrifiable composition (for example a glass frit) or a composition made vitreous (case, for example, where the composition forms the glass layer coating the pigments, as explained later).
- the glass composition of the printing paste according to the invention can therefore be in the form of a powder of a glass frit or of vitreous or vitrifiable coatings of the pigment grains.
- the printing paste may also comprise a glass composition in the form of the coatings of the pigments and one or more compositions in the form of glass frit powder (s).
- the coating of the nature of a glass or of a gel of the pigmentary grains may have a different composition or which corresponds, in whole or in part, to the composition of a glass frit of the printing paste.
- the printing paste comprises at least one glass composition with a low melting point, that is to say with a melting point lower than the deformation temperature of the glass of the substrate to be printed or at the baking temperature. of the printed substrate, that is to say in most cases less than 750-800 ° C. and generally less than 650 ° C.
- the coatings of the pigments have a low melting point (when, for example, the pigments used are sufficiently stable at the usual cooking temperatures of between 500 and 800 ° C.), it is possible to reduce the amount of composition of glass in the form of glass frit powder in the printing paste ready to bake or even to completely dispense with the contribution of this glass powder to the printing paste.
- the glass composition is then present in the printing paste in whole or in part in the form of glass coatings surrounding the pigments.
- a remarkably uniform and homogeneous distribution of the pigments in the baked enamel layer is automatically ensured, because neither accumulations of pigments nor large regions of pure glass matrix without coated pigments cannot form.
- the dough d printing according to the invention preferably comprises, in addition to the coatings, at least one composition in the form of a frit with a low melting point.
- the use according to the invention of pigments which are completely enclosed in a sealed coating of a thermally densified glass or gel as a preliminary stage of an appropriate glass has various favorable effects. For example, due to the coating, particles in principle more or less spherical with round or rounded surface are formed.
- Another essential advantage of the invention consists in that the printing paste, independently of the binder, largely contains grains or more or less spherical bodies having a glassy or vitrifiable surface.
- the invention therefore leads, even when using the colored pigments used up to now, to notable advantages as regards the quality of the layers of baked enamel. It also offers the advantage that the printing pastes, insofar as the glass composition is formed only by coating the grains of pigments, can be baked at lower temperatures. Indeed, in certain circumstances, it is not necessary to choose the high baking temperature to the point that the glass composition melts completely, but it may be sufficient in this case that the glass spheres containing a grain of pigment constitute by simple sintering a coherent layer. In this way, for example, more or less porous enamel layers can be obtained, which may be desirable in many cases.
- the invention also makes it possible to use colored pigments which are chemically less stable than the minerals with high melting point hitherto employed. Because the pigments are coated in a closed protective envelope, they do not come into immediate contact either with the ambient atmosphere or with any reactive agents in the printing paste during the baking process.
- the composition and the thickness of the protective coating of the nature of a glass or a gel must, in this case, be chosen so that the protective action remains intact at least for the duration of the operation. proper cooking.
- pigments which until now have been out of the question because they changed color or they completely lost their coloring function by oxidation or reduction during the cooking operation.
- colored pigments also iron oxides, such as magnetite (Fe 3 O 4 ) and / or hematite (Fe O 3 ), or even carbon in the form of carbon black or graphite or titanium nitride, etc.
- pigments which do not interfere when recycling glazed glass panes, because that they are completely burnt at the melting point of the glass and escape in the gaseous state, such as for example carbon or which dissolve in the molten glass and become constituents of the glasses in the form of oxides which are not bothersome, such as certain metal oxides.
- the protective coating of the nature of a glass or a gel around the pigments may consist of the oxides of the most diverse elements, in particular the oxides of the elements silicon, lead, bismuth, zinc, titanium, zirconium, aluminum, boron, phosphorus, calcium, magnesium, sodium and / or potassium.
- coatings of pure SiO 2 as well as coatings from the two-component system SiO 2 -B 2 O 3 in proportions of the order of 70 to 90% by weight of Si0 2 and from 10 to 30 % by weight of B 2 O 3 were found to be satisfactory.
- Coatings from the ternary system PbO-B 2 O 3 -SiO 2 in proportions of the order of 70 to 90% by weight of PbO, from 5 to 15% by weight of B 2 O 3 and from 5 to 15% by weight of SiO 2 or from the four-component system PbO- B 2 O 3 -SiO 2 -ZnO have also proved useful for the purposes of the invention, especially those from this four-component system in proportions of the from 65 to 92% by weight of PbO, from 5 to 20% by weight of B 2 O 3 , from 2 to 10% by weight of SiO 2 and from 1 to 5% by weight of ZnO.
- the coating of the colored pigments by means of the nature layer of a glass or a gel is carried out using the known sol-gel process, according to which the colored pigments are embedded in a soil which is densified by subsequent heat treatment in the field of the resulting glass transformation temperature.
- a printing paste based on a four-component glass d is prepared. following composition: 83.0% by weight of PbO, 13.0% by weight of B 2 O 3 , 2.4% by weight of SiO 2 and 1.6% by weight of ZnO, as low-point glass composition with a melting temperature of about 610 ° C, and copper chromite (CuCr 2 O 4 ) as a colored pigment.
- the glass composition must be present in the printing paste exclusively in the form of a coating of the nature of a glass or of the nature of a gel densified around the grains of pigments.
- the pigment and soil dispersion is subjected to a drying operation by blowing hot air or by “spraying” for which the temperature of the spray nozzle is maintained at 130 ° C.
- a black powder is obtained which consists of grains of the pigment coated with the dried gel.
- the gel layer contains residual organic radicals. These residual organic radicals are eliminated by a heat treatment of 2 hours at 475 ° C.
- the coating is thus simultaneously densified.
- 43 g of an organic binder for example a screen printing oil which contains 18% by weight of a resinous component and 82% by weight of a low volatile solvent such as l, are added to the powder obtained in this way. 'turpentine.
- the ready-to-use printing paste is obtained.
- the printing paste is applied according to the usual screen printing process to a sheet of float glass and dried for 5 minutes at a temperature between 120 and 180 ° C.
- the printed layer is baked at a temperature of about 600 ° C.
- the decorative layer of the nature of an enamel thus obtained consists of 50% of the glass component and 50% of the pigment.
- a printing paste based on a three-component glass having the following composition is prepared: 89.6% by weight of PbO, 5.2% by weight of B 2 O 3 and 5.2% by weight of SiO 2 as a composition of low melting point glass having a melting temperature of about 580 ° C, and of graphite as a colored pigment.
- the glass composition must be present in the printing paste again exclusively in the form of the coating of the nature of a glass on the graphite grains.
- a colorless transparent sol is prepared from 26.59 g of lead nitrate Pb (NO 3 ) 2 , from 100 ml of water, 2.6 ml of nitric acid 0.1 M, 3.61 g of tetraethoxysilane (TEOS) and 3.10 g of trimethyl borate (TMB) in 3.0 ml of ethanol.
- TEOS tetraethoxysilane
- TMB trimethyl borate
- the ready-to-use printing paste is obtained which is applied by the screen printing process to sheets of float glass and which is baked at baking temperatures between 500 and 700 ° C. Cullet with such enamel layers can be added to the mixture of a float glass melt without inconvenience because the carbon forming the colored pigment burns CO 2 in the molten glass and escapes upon gaseous state.
- a printing paste is prepared which contains a glass frit powder with low melting point as a glass composition and colored pigments formed by magnetite grains provided with a coating of glass with high melting point.
- the high melting point coating of the magnetite grains consists of a glass d bicomponent borosilicate having the composition of 83% by weight of B 2 O 3 and 17% by weight of SiO 2 and has a melting temperature of approximately 1110 ° C.
- the coating of glass with a high melting point does not melt during the cooking operation, but completely retains its protective action during this process and does not dissolve until a possible reflow of the cullet provided with the layer in the glass. molten during the recycling process.
- TEOS tetraethoxysilane
- TMB trimethyl borate
- the powder obtained in this way consisting of coated grains of pigment, is subjected to a heat treatment at a temperature of 700 ° C. in a nitrogen atmosphere with a heating rate of 1 K / min, a holding time of 1 hour. at 700 ° C, then a cooling rate of approximately 5 K / min.
- EXAMPLE 4 A printing paste is prepared as described in Example 3 which contains a low melting point frit in the form of glass powder, as well as colored pigments consisting of magnetite and which are coated with a layer.
- glass of high melting point formed of a borosilicate glass.
- the borosilicate glass consists of 84.1% by weight of B 2 O 3 and 15.9% by weight of SiO 2 and has a melting temperature of approximately 1130 ° C.
- the soil preparation is carried out in the same way as in Example 3, using in this case 7 ml of ethanol, in total 34.8 ml of 0.15 M hydrochloric acid, 93.87 g of tetraethoxysilane, 21.78 g of trimethyl borate and 20 g of magnetite powder. Spray drying is also carried out as described in the previous examples.
- the thermal post-treatment of the powder obtained after spray-drying with a view to densifying the coating of the nature of a gel with elimination of organic radicals takes place in this case at 800 ° C. in a nitrogen atmosphere.
- the temperature necessary for the oxidation of the magnetite moves from 280 ° C to 780 ° C, measured by differential thermal analysis at a heating rate of 10 K / min in the air.
- the pigment powder thus prepared formed by magnetite grains coated with glass is transformed into printing paste.
- Glass sheets with such enamel are recyclable and can be incorporated into the float glass mixture
- a printing paste is prepared which contains a low-melting glass frit in the form of glass powder, as well as colored pigments formed by magnetite which are surrounded by a coating of glass with high melting point.
- the glass coating consists in this case of a phosphoborosilicate glass having the composition of 67.4% by weight of SiO 2 , 21.7% by weight of P 2 O 5 and 10.9% by weight of B 2 O 3 .
- This glass has a melting temperature of around 1170 ° C.
- the soil preparation is carried out again in a similar manner to that of Example 1 using 20 ml of ethanol, 87.6 ml of hydrochloric acid
- TMB titanium dioxide
- TEOS TEOS
- hydrochloric acid a mixture of ethanol, TEOS and hydrochloric acids
- the TMB is added dropwise and the solution is stirred for 2 hours at 50 ° C.
- the remainder of the hydrochloric acid is then added, then the P 2 O 5 and finally the magnetite powder and dispersed for 5 minutes in an ultrasonic bath.
- the spray drying takes place as in Example 1.
- the powder obtained after spray drying and consisting of coated grains of pigment is subjected to heat treatment at 720 ° C. in an atmosphere of nitrogen with a heating speed of 1 K / min, a holding time at 720 ° C of 1 hour and a speed of cooling of approximately 5 K / min.
- the pigment powder thus prepared consisting of magnetite grains coated with glass, is converted in the manner described in Example 3 into a printing paste. Glass sheets coated with such enamel are recyclable and can be incorporated by mixing with the amount of float glass.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Geochemistry & Mineralogy (AREA)
- Ceramic Engineering (AREA)
- Wood Science & Technology (AREA)
- Glass Compositions (AREA)
Abstract
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP96920876A EP0777633A1 (fr) | 1995-06-08 | 1996-05-31 | Pate d'impression apte a la cuisson pour imprimer des surfaces de verre et procede pour fabriquer ladite pate |
JP9502684A JPH10504013A (ja) | 1995-06-08 | 1996-05-31 | ガラス表面に印刷するための焼成に適した印刷ペースト及び該ペーストの製造方法 |
CZ97404A CZ40497A3 (en) | 1995-06-08 | 1996-05-31 | Printing firing paste for printing on glass surfaces and process for producing thereof |
MXPA/A/1997/000914A MXPA97000914A (es) | 1995-06-08 | 1997-02-04 | Pasta de impresion que pude cocerse para imprimirsuperficies de vidrio y procesamiento para fabricar esa pasta |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19520964A DE19520964A1 (de) | 1995-06-08 | 1995-06-08 | Beschichtete anorganische Pigmente, Verfahren zu deren Herstellung und deren Verwendung |
DE19520964.8 | 1995-06-08 | ||
DE19525658A DE19525658C1 (de) | 1995-07-14 | 1995-07-14 | Einbrennbare Druckpaste zum Bedrucken von Glasoberflächen und Verfahren zur Herstellung der Druckpaste |
DE19525658.1 | 1995-07-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1996041773A1 true WO1996041773A1 (fr) | 1996-12-27 |
Family
ID=26015831
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/FR1996/000819 WO1996041773A1 (fr) | 1995-06-08 | 1996-05-31 | Pate d'impression apte a la cuisson pour imprimer des surfaces de verre et procede pour fabriquer ladite pate |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP0777633A1 (fr) |
JP (1) | JPH10504013A (fr) |
CZ (1) | CZ40497A3 (fr) |
PL (1) | PL318504A1 (fr) |
WO (1) | WO1996041773A1 (fr) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001021540A1 (fr) | 1999-09-23 | 2001-03-29 | Saint-Gobain Glass France | Vitrage muni d'un empilement de couches minces agissant sur le rayonnement solaire |
BE1013101A3 (fr) * | 1999-10-01 | 2001-09-04 | Solvay | Procede de traitement de pigments inorganiques. |
WO2007028913A1 (fr) | 2005-07-29 | 2007-03-15 | Saint-Gobain Glass France | Vitrage muni d'un empilement de couches minces agissant sur le rayonnement solaire |
WO2015145073A1 (fr) | 2014-03-28 | 2015-10-01 | Saint-Gobain Glass France | Vitrage muni d'un empilement de couches minces pour la protection solaire |
WO2019243755A1 (fr) * | 2018-06-22 | 2019-12-26 | Saint-Gobain Glass France | Feuille de verre revetue d'un empilement de couches minces et d'une couche d'email |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE69905495T3 (de) * | 1998-12-18 | 2008-09-25 | Ferro Gmbh | Bismuthmanganit-pigmente |
DE10049803A1 (de) * | 2000-10-09 | 2002-04-18 | Bayer Ag | Kompositpartikel |
JP7181841B2 (ja) * | 2018-07-11 | 2022-12-01 | 三ツ星ベルト株式会社 | セラミックカラーペースト、セラミックカラーならびにセラミックカラー付きガラスおよびその製造方法 |
Citations (11)
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DE2424599A1 (de) * | 1973-05-23 | 1974-12-12 | Mizusawa Industrial Chem | Ueberzogene pigmentzusammensetzung und verfahren zu ihrer herstellung |
JPS54156048A (en) * | 1978-05-31 | 1979-12-08 | Matsushita Electric Works Ltd | Synthetic resin molding compound |
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EP0603830A2 (fr) * | 1992-12-21 | 1994-06-29 | Central Glass Company, Limited | Composition colorante céramique et procédé de formation d'une couche colorante céramique sur une plaque de verre l'utilisant |
JPH07133211A (ja) * | 1993-11-11 | 1995-05-23 | Kira Keshohin Kk | 着色化粧品顔料 |
EP0665004A2 (fr) * | 1994-01-29 | 1995-08-02 | Lucky Ltd. | Pigment cosmétique anti-microbien, procédé de préparation et compositions cosmétiques le contenant |
EP0712813A1 (fr) * | 1994-11-21 | 1996-05-22 | Saint-Gobain Vitrage | Procédé d'émaillage de substrats en verre, composition d'émail utilisée et produits obtenus |
-
1996
- 1996-05-31 WO PCT/FR1996/000819 patent/WO1996041773A1/fr not_active Application Discontinuation
- 1996-05-31 JP JP9502684A patent/JPH10504013A/ja active Pending
- 1996-05-31 PL PL96318504A patent/PL318504A1/xx unknown
- 1996-05-31 CZ CZ97404A patent/CZ40497A3/cs unknown
- 1996-05-31 EP EP96920876A patent/EP0777633A1/fr not_active Withdrawn
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EP0455933A2 (fr) * | 1990-05-10 | 1991-11-13 | Degussa Aktiengesellschaft | Spinelles pigmentaires colorantes enrobées, procédé de fabrication et utilisation |
EP0569734A1 (fr) * | 1992-05-15 | 1993-11-18 | Cerdec Aktiengesellschaft Keramische Farben | Procédé de production de décorations à couleurs résistantes à la cuisson de la porcelaine et composition de pigments utile à cela |
EP0603830A2 (fr) * | 1992-12-21 | 1994-06-29 | Central Glass Company, Limited | Composition colorante céramique et procédé de formation d'une couche colorante céramique sur une plaque de verre l'utilisant |
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Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001021540A1 (fr) | 1999-09-23 | 2001-03-29 | Saint-Gobain Glass France | Vitrage muni d'un empilement de couches minces agissant sur le rayonnement solaire |
EP1947485A1 (fr) | 1999-09-23 | 2008-07-23 | Saint-Gobain Glass France | Vitrage muni d'un empilement de couches minces agissant sur le rayonnement solaire |
BE1013101A3 (fr) * | 1999-10-01 | 2001-09-04 | Solvay | Procede de traitement de pigments inorganiques. |
WO2007028913A1 (fr) | 2005-07-29 | 2007-03-15 | Saint-Gobain Glass France | Vitrage muni d'un empilement de couches minces agissant sur le rayonnement solaire |
WO2015145073A1 (fr) | 2014-03-28 | 2015-10-01 | Saint-Gobain Glass France | Vitrage muni d'un empilement de couches minces pour la protection solaire |
WO2019243755A1 (fr) * | 2018-06-22 | 2019-12-26 | Saint-Gobain Glass France | Feuille de verre revetue d'un empilement de couches minces et d'une couche d'email |
FR3082840A1 (fr) * | 2018-06-22 | 2019-12-27 | Saint-Gobain Glass France | Feuille de verre revetue d'un empilement de couches minces et d'une couche d'email. |
US11427501B2 (en) | 2018-06-22 | 2022-08-30 | Saint-Gobain Glass France | Glass sheet coated with a stack of thin layers and an with an enamel layer |
Also Published As
Publication number | Publication date |
---|---|
EP0777633A1 (fr) | 1997-06-11 |
PL318504A1 (en) | 1997-06-23 |
JPH10504013A (ja) | 1998-04-14 |
MX9700914A (es) | 1998-03-31 |
CZ40497A3 (en) | 1997-07-16 |
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