EP0015623B1 - Magnesium-Zusammensetzungen und Verfahren zur Bildung eines MgO-Films - Google Patents
Magnesium-Zusammensetzungen und Verfahren zur Bildung eines MgO-Films Download PDFInfo
- Publication number
- EP0015623B1 EP0015623B1 EP19800200206 EP80200206A EP0015623B1 EP 0015623 B1 EP0015623 B1 EP 0015623B1 EP 19800200206 EP19800200206 EP 19800200206 EP 80200206 A EP80200206 A EP 80200206A EP 0015623 B1 EP0015623 B1 EP 0015623B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- syrup
- organic
- magnesium
- solvent
- magnesium compound
- 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
Links
- 239000011777 magnesium Substances 0.000 title claims description 13
- 238000000034 method Methods 0.000 title claims description 11
- 229910052749 magnesium Inorganic materials 0.000 title claims description 9
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 title claims description 4
- 239000000203 mixture Substances 0.000 title description 16
- 239000006188 syrup Substances 0.000 claims description 40
- 235000020357 syrup Nutrition 0.000 claims description 40
- 150000002681 magnesium compounds Chemical class 0.000 claims description 24
- 239000002562 thickening agent Substances 0.000 claims description 21
- 239000002904 solvent Substances 0.000 claims description 20
- 229920000642 polymer Polymers 0.000 claims description 8
- 238000001035 drying Methods 0.000 claims description 7
- 238000007650 screen-printing Methods 0.000 claims description 6
- -1 magnesium carboxylate Chemical class 0.000 claims description 5
- 239000003960 organic solvent Substances 0.000 claims description 5
- 238000010304 firing Methods 0.000 claims description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 3
- AKTIAGQCYPCKFX-FDGPNNRMSA-L magnesium;(z)-4-oxopent-2-en-2-olate Chemical group [Mg+2].C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O AKTIAGQCYPCKFX-FDGPNNRMSA-L 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 239000010410 layer Substances 0.000 claims 3
- 125000005594 diketone group Chemical group 0.000 claims 1
- 239000011241 protective layer Substances 0.000 claims 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 50
- 239000000395 magnesium oxide Substances 0.000 description 26
- 229920000620 organic polymer Polymers 0.000 description 12
- 239000001856 Ethyl cellulose Substances 0.000 description 8
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 8
- 229920001249 ethyl cellulose Polymers 0.000 description 8
- 235000019325 ethyl cellulose Nutrition 0.000 description 8
- 238000000197 pyrolysis Methods 0.000 description 8
- 239000011521 glass Substances 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 238000003756 stirring Methods 0.000 description 5
- POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000004020 conductor Substances 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 238000004544 sputter deposition Methods 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- GZMAAYIALGURDQ-UHFFFAOYSA-N 2-(2-hexoxyethoxy)ethanol Chemical compound CCCCCCOCCOCCO GZMAAYIALGURDQ-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- 150000001242 acetic acid derivatives Chemical class 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 238000005305 interferometry Methods 0.000 description 2
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 125000004430 oxygen atom Chemical group O* 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- VXQBJTKSVGFQOL-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethyl acetate Chemical compound CCCCOCCOCCOC(C)=O VXQBJTKSVGFQOL-UHFFFAOYSA-N 0.000 description 1
- UVZMNGNFERVGRC-UHFFFAOYSA-N 4-cyclohexylbutanoic acid Chemical compound OC(=O)CCCC1CCCCC1 UVZMNGNFERVGRC-UHFFFAOYSA-N 0.000 description 1
- RVDLHGSZWAELAU-UHFFFAOYSA-N 5-tert-butylthiophene-2-carbonyl chloride Chemical compound CC(C)(C)C1=CC=C(C(Cl)=O)S1 RVDLHGSZWAELAU-UHFFFAOYSA-N 0.000 description 1
- 238000012935 Averaging Methods 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000000010 aprotic solvent Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- NJSUFZNXBBXAAC-UHFFFAOYSA-N ethanol;toluene Chemical compound CCO.CC1=CC=CC=C1 NJSUFZNXBBXAAC-UHFFFAOYSA-N 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 238000007496 glass forming Methods 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- UEGPKNKPLBYCNK-UHFFFAOYSA-L magnesium acetate Chemical compound [Mg+2].CC([O-])=O.CC([O-])=O UEGPKNKPLBYCNK-UHFFFAOYSA-L 0.000 description 1
- 235000011285 magnesium acetate Nutrition 0.000 description 1
- 239000011654 magnesium acetate Substances 0.000 description 1
- 229940069446 magnesium acetate Drugs 0.000 description 1
- QSMVRMKSCBMQIF-UHFFFAOYSA-L magnesium;4-cyclohexylbutanoate Chemical compound [Mg+2].[O-]C(=O)CCCC1CCCCC1.[O-]C(=O)CCCC1CCCCC1 QSMVRMKSCBMQIF-UHFFFAOYSA-L 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 238000000386 microscopy Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen 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
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 239000011819 refractory material Substances 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/02—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition
- C23C18/12—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition characterised by the deposition of inorganic material other than metallic material
- C23C18/1204—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition characterised by the deposition of inorganic material other than metallic material inorganic material, e.g. non-oxide and non-metallic such as sulfides, nitrides based compounds
- C23C18/1208—Oxides, e.g. ceramics
- C23C18/1216—Metal oxides
Definitions
- This invention relates to a screen-printable syrup and a method of firing this syrup to form a MgO film.
- British patent specification 1,455,148 discloses a method of forming a metallic (magnesium oxide) coating on a substrate wherein a solution of one or more metal acetates, halides and nitrates in an aprotic solvent having a dielectric constant greater than 15 and a dipole moment greater than 3 D is applied to the substrate and the metal compound (magnesium acetate) is pyrolyzed to form a transparent film of the metal oxide (magnesium oxide).
- M. O. Aboelfotoh and J. A. Lorenzen, "Influence of Secondary-Electron Emission from MgO Surfaces on Voltage-Breakdown Curves in Penning Mixtures for Insulated-Electrode Dischargers", J. Appl. Phys., Vol. 48, No. 11, 4754-4759 (1977) discloses the formation of a MgO film on the surface of an a-c plasma display panel by sputtering, which involves use of an electron gun to volatilize a magnesium compound and then deposit it as a MgO film on the surface of the panel to a thickness of about 3000 A.
- the disadvantage of this method of forming the MgO film is that sputtering is expensive.
- the present invention provides an anhydrous screen-printable syrup, comprising (a) an anhydrous organic magnesium compound pyrolyzable to a MgO film below 450°C and (b) an organic solvent, characterized in that the syrup further contains (c) a non carboxylated cellulosic polymer pyrolyzable below 450°C and in that the magnesium compound (a) and the polymer (c) are dissolved in the solvent (b) which is a non aqueous alcohol solvent, the syrup having a Brookfield viscosity of 3-200 Pa-S and provides further a more economical method of forming a film of MgO on a surface.
- the process of the invention for forming a MgO film on a surface is conducted by (a) screenprinting thereto a thin layer of the syrup of the invention, (b) drying the layer, and (c) firing the dried layer at a temperature below 450°C to volatilize the solvent (b) and to pyrolyze the thickener (c) and the organic magnesium compound (a).
- This process is useful in place of sputtering to form an MgO film on the surface of an a-c plasma display panel.
- composition of the present invention contains three essential ingredients, (a) an anhydrous organic magnesium compound pyrolyzable to a MgO film below 450°C, (b) a non-aqueous alcohol solvent and (c) a non-carboxylated cellulosic polymer pyrolyzable below 450°C, the syrup having a Brookfield-viscosity of 3-200 Pa-S.
- anhydrous organic magnesium compound pyrolyzable to a MgO film below 450°C
- a non-aqueous alcohol solvent a non-carboxylated cellulosic polymer pyrolyzable below 450°C
- the syrup having a Brookfield-viscosity of 3-200 Pa-S.
- the organic magnesium compound is selected so that it is pyrolyzable to MgO film and is soluble in the organic solvent used at ordinary room temperature. Selection of the organic magnesium compound can be subject to the pyrolysis temperature that can be used. For example, current surfaces of a-c plasma displays are made of lead-rich glass which undergoes a glass transition at a temperature above 450°C. To avoid this transition, the organic magnesium compound is pyrolyzable to MgO film at a temperature below 450°C.
- magnesium organic compounds examples include the oxygen-containing organic magnesium compounds such as magnesium carboxylates e.g. magnesium cyclohexanebutyrate, magnesium diketones, e.g. magnesium acetylacetonate, and magnesium alcoholates, e.g., magnesiumethoxide.
- oxygen-containing organic magnesium compounds such as magnesium carboxylates e.g. magnesium cyclohexanebutyrate, magnesium diketones, e.g. magnesium acetylacetonate, and magnesium alcoholates, e.g., magnesiumethoxide.
- magnesium carboxylates e.g. magnesium cyclohexanebutyrate
- magnesium diketones e.g. magnesium acetylacetonate
- magnesium alcoholates e.g., magnesiumethoxide.
- all the atoms bound to the magnesium atom in the compound are oxygen atoms and organic carbon atoms are bound to these oxygen atoms.
- the organic solvent component is selected so as to dissolve the remaining components of the syrup and to depart from the syrup without leaving any detectable residue during pyrolysis. Typically, most or all of the solvent will evaporate in a drying step preceding any heating to pyrolyze other components of the syrup. Such heating will also volatilize any remaining solvent.
- solvents examples include the glycol ethers, such as the Cellosolves@, e.g., methyl, butyl and hexyl, the Carbitols@, e.g., methyl, butyl, and hexyl, and the triglycols, e.g., methoxy, ethoxy, and butoxy, the alcohols, such as butanol and isopropanol, and the acetates, such as butyl carbitol acetate.
- glycol ethers such as the Cellosolves@, e.g., methyl, butyl and hexyl
- Carbitols@ e.g., methyl, butyl, and hexyl
- triglycols e.g., methoxy, ethoxy, and butoxy
- the alcohols such as butanol and isopropanol
- acetates such as butyl carbito
- the organic polymer thickener is selected so as to dissolve in the solvent that also dissolves the organic magnesium compound and to pyrolyze leaving no detectable residue which would prevent formation of the MgO film or would color it.
- thickeners are hydroxyethylcellulose, propoxyethylcellulose and ethylcellulose.
- the organic polymer thickener pyrolyzes to no detectable residue at temperatures up to 450°C.
- the syrup composition can be made by first dissolving the organic magnesium compound in the solvent and then dissolving the organic polymer thickener in the solution to get the syrup-like consistency desired. Without the organic polymer thickener, the solution would be too flowable to be screen printable. The polymer- free solution would just run through the screen onto the surface to be printed and then would spread out on such surface without producing the desired screen pattern.
- the thickening effect provided by the organic polymer thickener limits the flowability of the resultant syrup so that it can be screen printed by conventional thick-film paste screen printing techniques to a faithful reproduction of the screen image on the surface on which the syrup is screen printed.
- the organic magnesium compound and organic polymer thickener may not easily dissolve in the same solvent.
- this compound easily dissolves in hexyl Carbitol@ but ethyl cellulose thickener does not dissolve until heated for about one hour at 155°C. in the solvent, whereupon the polymer rapidly goes into solution.
- the syrup of the present invention is a solution, i.e., no solids are observable by the naked eye.
- This syrup differs from the usual screen printing media, in that such media normally contain solids.
- the organic polymer thickener generally imparts a viscosity of at least 3 Pa-S measured using a Brookfield viscometer at 10 rpm and 25°C. A viscosity greater than 200 Pa-S is generally not required.
- the organic polymer thickener does thicken the syrup, it does not prevent the MgO film from being formed upon pyrolysis, i.e., not only must the organic portion of the magnesium compound pyrolyze to MgO, but the organic polymer thickener must also pyrolyze at the same time without preventing formation of the MgO film.
- the pyrolysis products of the magnesium compound, except for MgO, and the organic polymer thickener, and any residue of the solvent after drying are volatile at the pyrolysis temperature used, so as to yield the colorless, transparent MgO film.
- the syrup of the present invention has a viscosity of from 10 Pa-S to 50 Pa-S.
- the syrup of the present invention will typically contain from 1 to 15% organic magnesium compound, 5 to 20% organic polymer thickener, and 65 to 90% solvent, all percents being by weight based on the total weight of these three components.
- Preferred compositions contain 4 to 8%, 6 to 15%, and 75 to 85% of organic magnesium compound, organic polymer thickener, and organic solvent, respectively.
- the amount of thickener is selected to give the syrup the viscosity desired; such amount will vary with the particular thickener selected and the inherent viscosity of the thickener.
- the proportion of components and viscosity are selected so as to give an MgO film upon screen printing and pyrolysis of at least about 1000 A.
- shelf life storage stability
- the components of the syrup are dried, preferably before combining into the composition. Drying can be done by heating and/or desiccation of each component.
- Organic magnesium compounds are available in hydrated form; the drying should remove the water of hydration from the compound.
- Solvents such as alcohols typically contain water, and this is most readily removed by desiccation in the presence of a desciccant such as CaCI 2 or mixing CaH 2 with the solvent at near its boiling point, followed by filtering out the CaH 2 particles.
- the resultant anhydrous or dried syrup has shelf life in excess of two months, whereas without drying, solids begin to appear after about three weeks storage.
- a preferred a-c plasma display panel is made by firing a thick silver conductor composition after printing in a conductor line pattern into a substrate, the composition comprising: (A) 50-85% of the weight of the composition, of silver particles of 0.05-20 micrometers in size; (B) 1-10% of the weight of the composition, of inorganic non-glass forming refractory materials or their precursors, such as aluminum oxide, zirconium oxide, cobalt/iron/chromium oxide, aluminium and copper, having a particle size range of 0.05-44 micrometers with at least 80% by weight of the particles in the 0.1-5 micrometer range; (c) 5-20% of the weight of the composition, of glass frit having a softening point range of 325-600°C such as lead borosilicate-based glass; and (D) 10-30% of the weight of the composition, of vehicle such as a UV polymerizable solution of polymethyl methacrylate and a polyfunctional monomer or a non-UV polymerizable solution of
- the overglaze composition preferably utilized contains a glass frit of the composition (mole %): PbO (68.2), Si0 2 (12.0), B 2 0 3 (14.1), and CdO (5.7), having a softening point of approximately 480°C.
- the overglaze composition dispersed in an ethyl cellulose-based vehicle, is screen printed over the fired conductor, dried, and then fired at a temperature and for a time sufficient to produce a clear, smooth coating. It is on this coating that the syrup of the present invention is printed and pyrolyzed.
- compositions and process of the present invention in which parts and percents are by weight unless otherwise indicated, are as follows:
- Example 2- One gram of Mg acetylacetonate was dissolved in 25 ml n-hexyl Carbitol@ while stirring on a hot plate. Then 2 grams ethyl cellulose of Ex. 1 was added and dissolved after standing for about one hour. The resultant syrup had a viscosity estimated to be between 10 to 50 Pa-S and was printed on glass slides, dried, and then fired at 460°C in a box furnace for 1 hour. The MgO films looked good by microscopy. Interferometry on three films indicated smoothness averaging 777 A thick.
- Example 3-Two grams of dried (125°C, 1 hour) Mg acetylacetonate was dissolved in 30 ml n-hexyl Carbitol by heating on a hot plate while stirring; 3 grams of ethyl cellulose of Ex. 1 was added and heating and stirring continued until dissolved. While hot, the solution was centrifuged to remove any undissolved material and impurities. The resultant syrup has a viscosity of about 50 Pa-S.
- the syrup was tested by screen printing on microscope slides, allowed to level for about 10 minutes, dried 10 minutes at 120°C and fired on a belt furance with a 20 minute, 450°C peak temperature.
- Thickness measurements shows 2058 A for two coats and 2711 A for three coats.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Ceramic Engineering (AREA)
- Inorganic Chemistry (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
- Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Claims (7)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US1840479A | 1979-03-07 | 1979-03-07 | |
| US18404 | 1979-03-07 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0015623A1 EP0015623A1 (de) | 1980-09-17 |
| EP0015623B1 true EP0015623B1 (de) | 1985-07-31 |
Family
ID=21787749
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP19800200206 Expired EP0015623B1 (de) | 1979-03-07 | 1980-03-04 | Magnesium-Zusammensetzungen und Verfahren zur Bildung eines MgO-Films |
Country Status (3)
| Country | Link |
|---|---|
| EP (1) | EP0015623B1 (de) |
| JP (1) | JPS55123657A (de) |
| DE (1) | DE3070913D1 (de) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59213664A (ja) * | 1983-05-13 | 1984-12-03 | 鐘淵化学工業株式会社 | セラミツクス前駆体フイルムおよびその製造法 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1521531A1 (de) * | 1965-07-23 | 1969-05-14 | Telefunken Patent | Verfahren zum Aufbringen von isolierenden UEberzuegen auf Metallteilen |
| IT996924B (it) * | 1972-12-21 | 1975-12-10 | Glaverbel | Procedimento per formare uno strato di ossido metallico |
-
1980
- 1980-03-04 DE DE8080200206T patent/DE3070913D1/de not_active Expired
- 1980-03-04 EP EP19800200206 patent/EP0015623B1/de not_active Expired
- 1980-03-07 JP JP2817980A patent/JPS55123657A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6338386B2 (de) | 1988-07-29 |
| DE3070913D1 (en) | 1985-09-05 |
| EP0015623A1 (de) | 1980-09-17 |
| JPS55123657A (en) | 1980-09-24 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4187340A (en) | Method of forming patterned transparent electro-conductive film on the substrate of liquid crystal display | |
| EP0524630A2 (de) | Zusammensetzung zur Verwendung in einem transparenten elektrisch leitenden Film sowie Verfahren zur Herstellung dieses Films | |
| JP2002524383A (ja) | アルカリ金属拡散障壁層 | |
| US4382980A (en) | Magnesium compositions and process for forming MGO film | |
| JP3338966B2 (ja) | 透明導電膜形成用塗布液 | |
| JP3521237B2 (ja) | 金属酸化物膜形成用組成物及びその製造法並びに金属酸化物膜の形成法 | |
| US4456549A (en) | Paste for formation of transparent electroconductive coating film and process for preparation of said paste | |
| EP0015623A1 (de) | Magnesium-Zusammensetzungen und Verfahren zur Bildung eines MgO-Films | |
| JP5028573B2 (ja) | 金属酸化物超微粒子を含有する透明導電膜形成用ペースト組成物 | |
| JP2965759B2 (ja) | 導電性薄膜形成用銀ペースト | |
| JP3049890B2 (ja) | 透明導電膜の形成方法 | |
| JPH09129141A (ja) | 金属酸化物薄膜形成用コーティング剤 | |
| JPH05314820A (ja) | 透明導電膜形成用組成物と透明導電膜形成方法 | |
| JPH0995627A (ja) | 金属酸化物薄膜形成用コーティング剤 | |
| JPS62297470A (ja) | 金属酸化物薄膜形成用ペ−スト | |
| JPH07118230B2 (ja) | 透明導電膜形成用ペ−スト状組成物および透明導電膜の形成方法 | |
| JP3091606B2 (ja) | 透明導電膜形成用組成物の作製方法および透明導電膜の形成方法 | |
| JPH02208373A (ja) | 有機銀パラジウムインク | |
| JPS6362117B2 (de) | ||
| JPS5899141A (ja) | 透明被膜形成用ペ−スト | |
| JPH0144788B2 (de) | ||
| JPS5927961A (ja) | 透明被膜形成用ペ−ストおよび透明被膜 | |
| JP3959861B2 (ja) | 透明導電膜形成方法 | |
| JPS6148589B2 (de) | ||
| JP3107095B2 (ja) | 抵抗体膜形成材料 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
| AK | Designated contracting states |
Designated state(s): CH DE FR GB IT NL SE |
|
| 17P | Request for examination filed |
Effective date: 19810112 |
|
| ITF | It: translation for a ep patent filed | ||
| GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
| AK | Designated contracting states |
Designated state(s): CH DE FR GB IT NL SE |
|
| REF | Corresponds to: |
Ref document number: 3070913 Country of ref document: DE Date of ref document: 19850905 |
|
| ET | Fr: translation filed | ||
| PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
| 26N | No opposition filed | ||
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 19901129 Year of fee payment: 12 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: SE Payment date: 19901204 Year of fee payment: 12 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: CH Payment date: 19901205 Year of fee payment: 12 Ref country code: DE Payment date: 19901205 Year of fee payment: 12 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 19901231 Year of fee payment: 12 |
|
| ITTA | It: last paid annual fee | ||
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: NL Payment date: 19910331 Year of fee payment: 12 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Effective date: 19920304 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SE Effective date: 19920305 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: CH Effective date: 19920331 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NL Effective date: 19921001 |
|
| GBPC | Gb: european patent ceased through non-payment of renewal fee | ||
| NLV4 | Nl: lapsed or anulled due to non-payment of the annual fee | ||
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Effective date: 19921130 |
|
| REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Effective date: 19921201 |
|
| REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST |
|
| EUG | Se: european patent has lapsed |
Ref document number: 80200206.3 Effective date: 19921005 |